This application is a national phase entry of PCT/CA2008/001253, filed Jul. 7, 2008, which claims priority from U.S. Provisional patent application Ser. No. 60/948,238 filed Jul. 6, 2007, each of these applications being incorporated herein in their entirety by reference.

FIELD OF THE DISCLOSURE

The present disclosure relates to the field of the stereoselective catalytic hydrogenations, in particular for the reduction of 4-tert-butylcyclohexanone to the corresponding alcohol, cis-4-tert-butylcyclohexanol.

BACKGROUND OF THE DISCLOSURE

Catalytic hydrogenation is a fundamental reaction in chemistry, and is used in a large number of chemical methods. Catalytic hydrogenation of ketones and aldehydes are useful and indispensable methods for the synthesis of alcohols, which are valuable end products and precursor chemicals in the pharmaceutical, agrochemical, flavor, fragrance, material and fine chemical industries.¹

The esters of 4-tert-butylcyclohexanol, and in particular, 4-tert-butylcyclohexyl acetate, are well known perfume ingredients. Cis-4-tert-butylcyclohexyl acetate is preferred in the perfume industry because of its intense woody odor with a flowery fragrance.²Cis-4-tert-butylcyclohexyl acetate is obtained by acetylation of the corresponding alcohol. Various methods have been used in the industry to selectively produce cis-4-tert-butylcyclohexanol by hydrogenation of 4-tert-butylcyclohexanone. These include the use of iridium³and rhodium⁴catalysts or the use of bulky borohydride reagents, such as lithium trisamylborohydride.⁵However, all of these methods suffer from significant drawbacks when applied on an industrial scale, for example, due to the low substrate catalyst ratios or the use of a very reactive reagent under stoichiometric conditions.

Noyori and co-workers developed hydrogenation conditions using the RuCl₂(PR₃)₂(diamine) hydrogenation catalyst system.⁶Noyori and co-workers also established a method for the production of cis-4-tert-butylcyclohexanol having 95-98% selectivity using the achiral catalyst RuCl₂(PPh₃)(en) and similar compounds.⁷

Ruthenium aminophosphine complexes of the type RuCl₂(aminophosphine)₂and RuCl₂(diphosphine)(aminophosphine) have been previously reported for the hydrogenation of ketones, aldehydes and imines.⁸

SUMMARY OF THE DISCLOSURE

It has now been found that the ruthenium aminophosphine complexes RuCl₂(aminophosphine)₂and RuCl₂(diphosphine)(aminophosphine) in the presence of a base are very effective catalysts for the stereoselective hydrogenation of 4-tert-butylcyclohexanone to produce cis-4-tert-butylcyclohexanol in high yields.

Therefore, the present disclosure includes a method for the production of cis-4-tert-butylcyclohexanol comprising contacting 4-tert-butylcyclohexanone with hydrogen gas, a catalyst comprising a ruthenium-aminophosphine complex and a base.

In an aspect of the disclosure, the method is characterized by the use of a ruthenium-aminophosphine complex of the formula (I):
RuX₂(PNH₂)_a(P₂)_bâ€ƒâ€ƒ(I)
wherein
X is any suitable anionic ligand and may be the same or different;
a is 1 or 2:
b is 0 or 1, where a+b=2;
(PNH₂) represents an aminophosphine ligand of formula (II):
R¹R²P-L-NH₂â€ƒâ€ƒ(II)
(P₂) represents a diphosphine ligand of the formula III
R³R⁴P-L-PR⁵R⁶â€ƒâ€ƒ(III)
wherein
R¹, R², R³, R⁴, R⁵and R⁶are simultaneously or independently selected from H, C_1-20alkyl, C_2-20alkenyl, C_2-20alkynyl, C_3-20cycloalkyl, C_3-20cycloalkenyl, C_6-14aryl, heteroaryl, OR⁷and NR⁷R⁸, said latter 9 groups being optionally substituted, or R¹and R²and/or R³and R⁴and/or R⁵and R⁶are linked together to form an optionally substituted monocyclic or polycyclic ring system having 4 or more atoms, including the phosphorous atom to which said groups are bonded, and in which one or more carbon atoms in said monocyclic or polycyclic ring system is optionally replaced with a heteromoiety selected from O, S, N, NR⁷, SiR⁷and SiR⁷R⁸;
L is selected from C_1-10alkylene, C_2-10-alkenylene, C_2-10alkynylene, (C_6-14arylene)_m, C_1-10alkylene-C_6-14arylene, C_6-14arylene-C_1-10alkylene and C_1-10alkylene-(C_6-14arylene)_m-C_1-10alkylene, said latter 7 groups being optionally substituted;
m is 1, 2 or 3;
the optional substituents are selected from one or more of halo, OR⁷, NR⁷R⁸and R⁹; and
R⁷and R⁸are simultaneously or independently selected from H, fluoro-substituted-C_1-6alkyl, C_1-6alkyl, C_2-6alkenyl, C_2-6alkynyl, C_6-14aryl and C_1-6alkylene-C_6-14aryl; and
R⁹is selected from fluoro-substituted-C_1-6alkyl, C_1-6alkyl, C_2-6alkenyl, C_2-6alkynyl, C_6-14aryl and C_1-6alkylene-C_6-14aryl.

Other features and advantages of the present disclosure will become apparent from the following detailed description. It should be understood, however, that the detailed description and the specific examples while indicating preferred embodiments of the disclosure are given by way of illustration only, since various changes and modifications within the spirit and scope of the disclosure will become apparent to those skilled in the art from this detailed description.

BRIEF DESCRIPTION OF THE DRAWINGS

The disclosure will now be described in greater detail with reference to the following drawings in which:

FIG. 1 shows the preparation of a ruthenium-aminophosphine complex in an embodiment of the present disclosure.

FIG. 2 shows the structure of ruthenium complexes in embodiments of the disclosure.

FIG. 3 shows the reduction of 4-tertbutylcyclohexanol in an embodiment of the disclosure.

DETAILED DESCRIPTION OF THE DISCLOSUREDefinitions

The term â€œC_1-nalkylâ€ as used herein means straight and/or branched chain, saturated alkyl groups containing from one to â€œnâ€ carbon atoms and includes (depending on the identity of n) methyl, ethyl, propyl, isopropyl, n-butyl, s-butyl, isobutyl, t-butyl, 2,2-dimethylbutyl, n-pentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, n-hexyl and the like, where the variable n is an integer representing the largest number of carbon atoms in the alkyl group.

The term â€œC_2-nalkenylâ€ as used herein means straight and/or branched chain, unsaturated alkyl groups containing from two to n carbon atoms and one or more, suitably one to three, double bonds, and includes (depending on the identity of n) vinyl, allyl, 2-methylprop-1-enyl, but-1-enyl, but-2-enyl, but-3-enyl, 2-methylbut-1-enyl, 2-methylpent-1-enyl, 4-methylpent-1-enyl, 4-methylpent-2-enyl, 2-methylpent-2-enyl, 4-methylpenta-1,3-dienyl, hexen-1-yl and the like, where the variable n is an integer representing the largest number of carbon atoms in the alkenyl group.

The term â€œC_2-nalkynylâ€ as used herein means straight and/or branched chain, unsaturated alkyl groups containing from one to n carbon atoms and one or more, suitably one to three, triple bonds, and includes (depending on the identity of n) ethynyl, 1-propynyl, 2-propynyl, 2-methylprop-1-ynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1,3-butadiynyl, 3-methylbut-1-ynyl, 4-methylbut-ynyl, 4-methylbut-2-ynyl, 2-methylbut-1-ynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1,3-pentadiynyl, 1,4-pentadiynyl, 3-methylpent-1-ynyl, 4-methylpent-2-ynyl-4-methylpent-2-ynyl, 1-hexynyl and the like, where the variable n is an integer representing the largest number of carbon atoms in the alkynyl group.

The term â€œC_3-ncycloalkylâ€ as used herein means a monocyclic or polycyclic saturated carbocylic group containing from three to n carbon atoms and includes (depending on the identity of n), cyclopropyl, cyclobutyl, cyclopentyl, cyclodecyl, bicyclo[2.2.2]octane, bicyclo[3.1.1]heptane and the like, where the variable n is an integer representing the largest number of carbon atoms in the cycloalkyl group.

The term â€œC_3-ncycloalkenylâ€ as used herein means a monocyclic or polycyclic carbocylic group containing from three to n carbon atoms and one or more, suitably one or two, double bonds and includes (depending on the identity of n), cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclodecevyl, bicyclo[2.2.2]oct-2-ene, bicyclo[3.1.1]hept-2-ene and the like, where the variable n is an integer representing the largest number of carbon atoms in the cycloalkenyl group.

The term â€œC_6-narylâ€ as used herein means a monocyclic or polycyclic carbocyclic ring system containing from 6 to n carbon atoms, at least one aromatic ring and optionally a metal and includes, depending on the identity of n, phenyl, naphthyl, anthracenyl, 1,2-dihydronaphthyl, 1,2,3,4-tetrahydronaphthyl, fluorenyl, indanyl, indenyl, ferrocenyl and the like, where the variable n is an integer representing the largest number of carbon atoms in the aryl group.

The term â€œheteroarylâ€ as used herein means a monocyclic or polycyclic ring system containing one or two aromatic rings and from 5 to 14 atoms of which, unless otherwise specified, one, two, three, four or five are heteromoieties independently selected from N, NR⁷, NR⁷R⁸, O, S, SiR⁷and SiR⁷R⁸, wherein R⁷and R⁸are as defined for formula (III), and includes thienyl, furyl, pyrrolyl, pyrididyl, indolyl, quinolyl, isoquinolyl, tetrahydroquinolyl, benzofuryl, benzothienyl and the like.

The term â€œfluoro-substitutedâ€ with respect to any specified group as used herein means that the one or more, including all, of the hydrogen atoms in the group have been replaced with a fluorine, and includes trifluoromethyl, pentafluoroethyl, fluoromethyl and the like.

The suffix â€œeneâ€ added on to any of the above groups means that the group is divalent, i.e. inserted between two other groups.

The term â€œring systemâ€ as used herein refers to a carbon-containing ring system, that includes monocycles and bridged rings. Where specified, the carbons in the rings may be substituted or replaced with heteroatoms. Ring system include saturated, unsaturated or aromatic rings, or mixtures thereof.

The term â€œpolycyclicâ€ as used herein means groups that contain more than one ring linked together and includes, for example, groups that contain two (bicyclic), three (tricyclic) or four (quadracyclic) rings. The rings may be linked through a single bond, a single atom (spirocyclic) or through two atoms (fused and bridged).

In understanding the scope of the present disclosure, the term â€œcomprisingâ€ and its derivatives, as used herein, are intended to be open ended terms that specify the presence of the stated features, elements, components, groups, integers, and/or steps, but do not exclude the presence of other unstated features, elements, components, groups, integers and/or steps. The foregoing also applies to words having similar meanings such as the terms, â€œincludingâ€ , â€œhavingâ€ and their derivatives. Finally, terms of degree such as â€œsubstantiallyâ€ , â€œaboutâ€ and â€œapproximatelyâ€ as used herein mean a reasonable amount of deviation of the modified term such that the end result is not significantly changed. These terms of degree should be construed as including a deviation of at least Â±5% of the modified term if this deviation would not negate the meaning of the word it modifies.

Method of the Disclosure

It has been found that the ruthenium aminophosphine complexes RuCl₂(aminophosphine)₂and RuCl₂(diphosphine)(aminophosphine) in the presence of a base are very effective catalysts for the stereoselective hydrogenation of 4-tert-butylcyclohexanone, producing cis-4-tert-butylcyclohexanol in high yields.

Accordingly, the present disclosure relates to a method for the production of cis-4-tert-butylcyclohexanol comprising contacting 4-tert-butylcyclohexanone with hydrogen gas, a catalyst comprising a ruthenium-aminophosphine complex and a base.

In an aspect of the disclosure, the method is characterized by the use of a ruthenium-aminophosphine complex of the formula (I):
RuX₂(PNH₂)_a(P₂)_bâ€ƒâ€ƒ(I)
wherein
X is a suitable anionic ligand and may be the same or different;
a is 1 or 2:
b is 0 or 1, where a+b=2;
(PNH₂) represents an aminophosphine ligand of formula (II):
R¹R²P-L-NH₂â€ƒâ€ƒ(II)
(P₂) represents a diphosphine ligand of the formula III
R³R⁴P-L-PR⁵R⁶â€ƒâ€ƒ(III)
wherein
R¹, R², R³, R⁴, R⁵and R⁶are simultaneously or independently selected from H, C_1-20alkyl, C_2-20alkenyl, C_2-20alkynyl, C_3-20cycloalkyl, C_3-20cycloalkenyl, C_6-14aryl, heteroaryl, OR⁷and NR⁷R⁸, said latter 9 groups being optionally substituted, or R¹and R²and/or R³and R⁴and/or R⁵and R⁶are linked together to form an optionally substituted monocyclic or polycyclic ring system having 4 or more atoms, including the phosphorous atom to which said groups are bonded, and in which one or more carbon atoms in said monocyclic or polycyclic ring system is optionally replaced with a heteromoiety selected from O, S, N, NR⁷, SiR⁷and SiR⁷R⁸;
L is selected from C_1-10alkylene, C_2-10-alkenylene, C_2-10-alkynylene, (C_6-14arylene)_m, C_1-10alkylene-C_6-14arylene, C_6-14arylene-C_1-10alkylene and C_1-10alkylene-(C_6-14arylene)_m-C_1-10alkylene, said latter 7 groups being optionally substituted;
m is 1, 2 or 3;
the optional substituents are selected from one or more of halo, OR⁷, NR⁷R⁸and R⁹; and
R⁷and R⁸are simultaneously or independently selected from H, fluoro-substituted-C_1-6alkyl, C_1-6alkyl, C_2-6alkenyl, C_2-6alkynyl, C_6-14aryl and C_1-6alkylene-C_6-14aryl; and
R⁹is selected from fluoro-substituted-C_1-6alkyl, C_1-6alkyl, C_2-6alkenyl, C_2-6alkynyl, C_6-14aryl and C_1-6alkylene-C_6-14aryl.

In the present disclosure, a is equal to 1 or 2 and b is equal to 0 or 1, wherein a+b=2. In embodiments of the disclosure, a is equal to 2.

In an embodiment of the present disclosure R¹, R², R³, R⁴, R⁵and R⁶are simultaneously or independently selected from H, C_1-10alkyl, C_2-10-alkenyl, C_2-10alkynyl, C_3-10cycloalkyl, C_3-10cycloalkenyl, C_6-10-aryl, heteroaryl, OR⁷and NR⁷R⁸, said latter 9 groups being optionally substituted, or R¹and R²and/or R³and R⁴and/or R⁵and R⁶are linked together to form an optionally substituted monocyclic or bicyclic, saturated, unsaturated and/or aromatic ring system having 4 to 14 atoms, including the phosphorous atom to which said groups are bonded, and in which one or more carbon atoms in said monocyclic or polycyclic ring system is optionally replaced with a heteromoiety selected from O, S, N, NH and NC_1-4alkyl. In a further embodiment, R¹, R², R³, R⁴, R⁵and R⁶are simultaneously or independently selected from H, C_1-6alkyl, C_2-6alkenyl, C_2-6alkynyl, C_3-6cycloalkyl, C_3-6cycloalkenyl and C_6-10aryl said latter 6 groups being optionally substituted, or R¹and R²and/or R³and R⁴and/or R⁵and R⁶are linked together to form an optionally substituted monocyclic or bicyclic, saturated, unsaturated and/or aromatic ring system having 4 to 10 atoms, including the phosphorous atom to which said groups are bonded. In another embodiment of the disclosure R¹, R², R³, R⁴, R⁵and R⁶are simultaneously or independently selected from H, C_1-6alkyl, C_2-6alkenyl, C_2-6alkynyl, C_3-6cycloalkyl, and C_6-10aryl said latter 6 groups being optionally substituted, or R¹and R²and/or R³and R⁴and/or R⁵and R⁶are linked together to form an optionally substituted monocyclic or bicyclic, saturated, unsaturated and/or aromatic ring system having 4 to 10 atoms, including the phosphorous atom to which said groups are bonded. In specific embodiments of the disclosure, R¹, R², R³, R⁴, R⁵and R⁶are simultaneously or independently selected from phenyl and C_1-6alkyl, suitably, phenyl, methyl, ethyl, n-propyl, isopropyl, sec-butyl, tert-butyl and n-butyl.

In an embodiment of the disclosure, L is selected from C_1-6alkylene, C_2-6alkenylene and (C_6-14arylene)_m, said latter 3 groups being optionally substituted and m is 1 or 2. In a further embodiment L is unsubstituted C_1-6alkylene, suitably unsubstituted C_1-4alkylene, more suitably unsubstituted C_2-3alkylene. In a further embodiment, L is optionally substituted biphenyl or binaphthyl, more suitably unsubstituted biphenyl or binaphthyl. In another embodiment of the disclosure the biphenyl has a bond between the 2 and 2â€² positions and the binaphthyl has a bond between the 2 and 2â€² positions.

According to embodiments of the disclosure, the optional substituents on the aminophosphine and diphosphine ligands of formulae II and III are selected from one or more of halo, OH, NH₂, NHR⁷, OR⁷, N(R⁷)(R⁸) and R⁹, in which R⁷, R⁸and R⁹are simultaneously or independently selected from fluoro-substituted-C_1-6alkyl, C_1-6alkyl, C_2-6alkenyl, C_2-6alkynyl and C_6-14aryl. In embodiments of the disclosure, the optional substituents are selected from one or more of halo, OH, NH₂, NHR⁷, OR⁷, NR⁷R⁸and R⁹, in which R⁷, R⁸and R⁹are simultaneously or independently selected from fluoro-substituted-C_1-4alkyl, C_1-4alkyl, C_2-4alkenyl and phenyl, specifically methyl and phenyl.

The ligands X may be the same or different and are selected from any anionic ligand, suitably halo (for example, fluoro, chloro, bromo or iodo, specifically chloro), HO^âˆ’, R⁹O^âˆ’ and R⁹C(O)^âˆ’, wherein R⁹is H or C_1-6alkyl. In an embodiment of the disclosure, X is chloro.

In a general way, the complexes of the aminophosphine and diphosphine ligands of formulae II and III can be prepared and isolated prior to their use in the method according to the general methods described in the literature (see for example, Clarke, Z. E. et al. Organometallics, 2006, 25:4113-4117) or using the methods described herein.

The ruthenium complexes of formula (I) can catalytically hydrogenate 4-tertbutylcyclohexanone in the presence of a base. The base can be any conventional base and one can cite, as non-limiting examples, organic non-coordinating bases such as DBU, an alkaline or alkaline-earth metal carbonate, a carboxylate salt such as sodium or potassium acetate, or an alcoholate or hydroxide salt. In an embodiment of the disclosure, the bases are the alcoholate or hydroxide salts selected from of the compounds of formula (R¹⁰O)₂Mâ€² and R¹⁰OMâ€², wherein Mâ€² is an alkaline or alkaline-earth metal and R¹⁰stands for hydrogen or a linear or branched alkyl group. In a further embodiment of the disclosure, R¹⁰is t-butyl and Mâ€² is potassium.

Standard catalytic hydrogenation conditions, as used herein, typically implies the mixture of the substrate with a ruthenium-aminophosphine compound of formula (I) in the presence of a base, with a solvent, and then treating such a mixture with a hydrogen gas at a chosen pressure and temperature.

In an embodiment of the disclosure the hydrogen gas is used at a pressure of about 1 atm to about 100 atm, suitably about 7 atm to about 13 atm, more suitably about 10 atm.

The complexes of formula (I) can be added to the reaction medium in a large range of concentrations. As non-limiting examples, one can cite as complex concentration values those ranging from 0.1 ppm to 50,000 ppm, relative to the amount of substrate, thus representing respectively a substrate/complex (S/com or S/C) ratio of 10⁷to 20. In an embodiment of the disclosure, the complex concentration will be comprised between 0.1 and 1000 ppm, i.e. a S/com ratio of 10⁷to 1000 respectively. In a further embodiment of the disclosure, there will be used concentrations in the range of 0.5 to 100 ppm, corresponding to a S/com ratio of 10,000 to 2Ã—10⁶respectively.

In an embodiment of the disclosure, the base may be included in a relatively large range. One can cite, as non-limiting examples, ranges between 1 to 50,000 molar equivalents relative to the complex (e.g. base/com=0.5 to 50,000), or 100 to 20,000, or even between 400 and 10,000 molar equivalents. However, it should be noted that it is also possible to add a small amount of base (e.g. base/com=1 to 3) to achieve high yields.

In an embodiment of the present disclosure, the catalytic hydrogenation reaction is carried out in the presence of a solvent. A wide variety of solvents can be used for the catalytic hydrogenation. Non-limiting examples include aromatic solvents such as benzene, toluene or xylene, hydrocarbon solvents such as hexane or cyclohexane, ethers and esters such as tetrahydrofuran, diethyl ether and ethyl acetate, primary or secondary alcohols such as methanol, ethanol and isopropanol, chlorinated solvents such as dichloromethane and chloroform, or mixtures thereof.

The temperature at which the catalytic hydrogenation can be carried out is comprised between about 0Â° C. and about 100Â° C., more specifically in the range of between about 20Â° C. and about 80Â° C. In an embodiment of the disclosure, the catalytic hydrogenation is carried out at about room temperature. Of course, a person skilled in the art is also able to select the temperature as a function of the melting and boiling point of the starting and final products.

The following non-limiting examples are illustrative of the present disclosure:

EXAMPLES

All preparations and manipulations were carried out under hydrogen or argon atmospheres with the use of standard Schlenk, vacuum line and glove box techniques in dry, oxygen-free solvents. Tetrahydrofuran (THF), diethyl ether (Et₂O) and hexanes were purified and dried using an Innovative Technologies solvent purification system. Deuterated solvents were degassed and dried before use. Potassium tert-butoxide, aldehydes and ketones were supplied by Aldrich Chemical Company. NMR spectra were recorded on either a Varian Unity Inova 300 MHz spectrometer (300 MHz for ¹H, 75 MHz for ¹³C and 121.5 for ³¹P) or a Bruker Avance 500 MHz DRX spectrometer. All ³¹P chemical shifts were measured relative to 85% H₃PO₄as an external reference. The ¹H and ¹³C chemical shifts were measured relative to partially deuterated solvent peaks but are reported relative to tetramethylsilane. The alcohol products obtained from the catalytic hydrogenation of ketones were characterized by their ¹H and ¹³C NMR spectra. The aminophosphine ligands ⁱPr₂PCH₂CH₂NH₂and Ph₂PCH₂CH₂NH₂, and the ruthenium complexes RuCl₂(Ph₂PCH₂CH₂NH₂)₂, RuCl₂(R-binap)(Ph₂PCH₂CH₂NH₂) and RuCl₂(ⁱPr₂PCH₂CH₂NH₂)₂are commercially available from Kanata Chemical Technologies Inc.

Example 1Preparation of RuCl₂(ⁱPr₂PCH₂CH₂NH₂)₂(3)

A mixture of RuCl₂(cod)]_n(1.0 mmol) and the aminophosphine ligand ⁱPr₂PCH₂CH₂NH₂(2.1 mmol) was refluxed in toluene (40 ml) under argon for 12 hours. The mixture was cooled to room temperature and stirred for 6 hours. Ether (100 ml) was added, and the mixture stirred for 2 hours. The product was filtered, washed with ether (3Ã—10 ml), and dried under vacuum. Yield=93%. ¹H NMR (CD₂Cl₂), d: 1.17-1.38 (m, 24H, CH₃); 2.00 (m, 4H, CH₂); 2.52 (doublet of septet, J_HP=9.3 Hz, J_HH=10.5 Hz, 4H, CH); 3.06 (m, 4H, CH₂); 3.65 (br, 4H, NH). ³¹P{¹H} NMR (CD₂Cl₂), d: 64.2 (s).

Example 2General Procedure for Catalytic Hydrogenation of Ketones and Aldehydes

In a typical catalytic hydrogenation procedure, a weighed amount of the respective ruthenium catalyst and KO^tBu were added to a solution of the substrate in 2-propanol under hydrogen gas. The pressure was adjusted to the desired value and the reaction progress was monitored using TLC or NMR. After completion of the reaction, the solvent was removed by evaporation under reduced pressure. The alcohols were purified by filtering a hexane solution of the crude product through a pad of silica, then removing the hexane under reduced pressure. The conversion and purity of the alcohol products was assessed using NMR.

Discussion

The ruthenium aminophosphine complexes RuCl₂(Ph₂PCH₂CH₂NH₂)₂(1) and RuCl₂(R-binap)(Ph₂PCH₂CH₂NH₂) (2) were prepared as previously described.⁷Table 1 shows the hydrogenation of ketones using the ruthenium-aminophosphine complex, RuCl₂(i-Pr₂PCH₂CH₂NH₂)₂(3), to prove its efficacy as a catalyst for hydrogenation.

Table 2 shows the hydrogenation of 4-tert-butylcyclohexanone using catalysts (1), (2) and (3) (see FIG. 2) in the presence of a base. Catalyst (3) shows a cis:trans selectivity of 96:4 for the production of cis-4-tert-butylcyclohexanol.

The results show that the ruthenium-aminophosphine complexes of the present disclosure represent a very effective class of catalysts for hydrogenation of 4-tert-butyl cyclohexanone. The ketone was readily converted to the alcohol using each of the complexes (1, 2 and 3) as catalyst in the presence of base. Good selectivity was obtained for the desired cis-4-tert-butyl cyclohexanol, in particular with catalyst 3.

Example 3Catalytic Hydrogenation of 4-tert-butylcyclohexanone with RuCl₂(i-Pr₂PCH₂CH₂NH₂)₂(3)

(a) Substrate:Catalyst Ratio of 10,000:1

A weighed amount of the catalyst (3.2 mg, 0.0065 mmol) and KO^tBu (100 mg) were added to a solution of the substrate (10.0 g, 65 mmol) in 2-propanol in a 100 ml Parr pressure reactor under a flow of argon. The mixture was de-gassed with argon and then with hydrogen. It was finally pressurized to 10 atm. of hydrogen and stirred at the desired temperature. Yields are based on the amount of substrate and are shown in Table 3.
(b) Substrate:Catalyst Ratio of 100,000:1
A weighed amount of the catalyst (5 mg) was dissolved in 10.0 ml of 2-propanol. An aliquot of 1.0 ml of the diluted catalyst solution (0.5 mg of catalyst, 0.001 mmol) and KO^tBu (150 mg) were added to a solution of the substrate (15.6 g, 101 mmol) in 2-propanol in a 100 ml Parr pressure reactor under a flow of argon. The mixture was de-gassed with argon and then with hydrogen. It was finally pressurized to 10 atm. of hydrogen and stirred at the desired temperature. Yields are based on the amount of substrate and are shown in Table 3.
(c) Substrate:Catalyst Ratio of 500,000:1
A weighed amount of the catalyst (5 mg) was dissolved in 10.0 ml of 2-propanol. An aliquot of 1.0 ml of this catalyst solution was further diluted to 10.0 ml with 2-propanol. An aliquot of 2.0 ml of the dilute catalyst solution (0.1 mg, 0.0002 mmol) and KO^tBu (150 mg) were added to a solution of the substrate (15.6 g, 101 mmol) in 2-propanol in a 100 ml Parr pressure reactor under a flow of argon. The mixture was de-gassed with argon and then with hydrogen. It was finally pressurized to 10 atm. of hydrogen and stirred at the desired temperature. Yields are based on the amount of substrate.
(d) Substrate:Catalyst Ratio of 1,000,000:1
A weighed amount of the catalyst (5 mg) was dissolved in 10.0 ml of 2-propanol. An aliquot of 1.0 ml of this catalyst solution was further diluted to 10.0 ml with 2-propanol. An aliquot of 1.0 ml of the dilute catalyst solution (0.05 mg, 0.0001 mmol) and KO^tBu (150 mg) were added to a solution of the substrate (15.6 g, 101 mmol) in 2-propanol in a 100 ml Parr pressure reactor under a flow of argon. The mixture was de-gassed with argon and then with hydrogen. It was finally pressurized to 10 atm. of hydrogen and stirred at the desired temperature. Yields are based on the amount of substrate.
Discussion
Table 3 shows the hydrogenation of 4-tert-butylcyclohexanone using catalyst (3) in varying substrate:catalyst ratios, in the presence of a base. Catalyst (3) shows a cis:trans selectivity of at least 95:5 for the production of cis-4-tert-butylcyclohexanol, and 100% conversion for the 10,000/100,000/500,000:1 ratios of substrate:catalyst.

While the present disclosure has been described with reference to what are presently considered to be the preferred examples, it is to be understood that the disclosure is not limited to the disclosed examples. To the contrary, the disclosure is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims.

All publications, patents and patent applications are herein incorporated by reference in their entirety to the same extent as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated by reference in its entirety. Where a term in the present application is found to be defined differently in a document incorporated herein by reference, the definition provided herein is to serve as the definition for the term.

TABLE 1HYDROGENATION OF KETONES USINGRuCl₂(i-Pr₂PCH₂CH₂NH₂)₂/t-BuOK (1:10) AS CATALYST IN2-PROPANOL (10 ATM. H₂) AT ROOM TEMPERATURE.^atimeconventrysubstrateS:C(h)(%)1 [Image Omitted]

50001.5100 â€‚4^b [Image Omitted]

5003100 â€‰â€‰6^c [Image Omitted]

6506100^aA weighed amount of the catalyst and KO^tBu were added to a solution of the substrate in 2-propanol and the mixture stirred at room temperature under hydrogen gas. Yields are based on the amount of substrate.^bOnly carbonyl group is reduced;^cratio of endo:exo = 87:13.

TABLE 2HYDROGENATION OF 4-TERT-BUTYLCYCLOHEXANONE USING 1, 2 AND 3 ASCATALYST IN 2-PROPANOL (10 ATM. H₂) ATROOM TEMPERATURE.^aentrycatalystS:Ctime (h)conv (%)cis:trans111000210086:14221000610090:10331000210096:4â€‚^aA weighed amount of the catalyst and KO^tBu were added to a solution of the substrate in 2-propanol and the mixture stirred at room temperature under hydrogen gas. Yields are based on the amount of substrate.

TABLE 3HYDROGENATION OF 4-TERT-BUTYLCYCLOHEXANONEUSING 3 AS CATALYST IN 2-PROPANOL (10 ATM. H₂). [Image Omitted]

Conv.EntryS:CTemp. (Â° C.)Time (h)(%)Cis/Trans110,00020410096/42100,00050210095/53500,000501210095/541,000,00050248095/5

FULL CITATIONS FOR DOCUMENTS REFERRED TO IN THE SPECIFICATION

(1) (a) Mikami, K.; Korenaga, T.; Terada, M.; Ohkuma, T.; Pham, T.; Noyori, R. Angew. Chem., Int. Ed. 1999, 38, 495-497. (b) Doucet, H.; Ohkuma, T.; Murata, K.; Yokozawa, T.; Kozawa, M.; Katayama, E.; England, A. F.; Ikariya, T.; Noyori, R. Angew. Chem., Int. Ed. 1998, 37, 1703-1707. (c) Ohkuma, T.; Ooka, H.; Ikariya, T.; Noyori, R. J. Am. Chem. Soc. 1995, 117, 10417-10418.
(2) Arctander, S. 1969, Perfume and Flavor Chemicals, Montclair, N.J., Monograph No. 441.
(3) Eliel, E. L.; Doyle, T. W.; Hutchins, R. O.; Gilbert, E. C. Organic Syntheses 1970, 50, 13-15.
(4) Nishimura, S.; Ishige, M.; Shiota, M. Chemistry Letters 1977, 963-966.
(5) Krishnamurthy, S.; Brown, H. C. J. Am. Chem. Soc. 1976, 98, 3383-3384.
(6) (a) Mikami, K.; Korenaga, T.; Terada, M.; Ohkuma, T.; Pham, T.; Noyori, R. Angew. Chem., Int. Ed. 1999, 38, 495-497. (b) Ohkuma, T.; Ooka, H.; Ikariya, T.; Noyori, R. J. Am. Chem. Soc. 1995, 117, 10417-10418.
(7) (a) Doucet, H.; Ohkuma, T.; Murata, K.; Yokozawa, T.; Kozawa, M.; Katayama, E.; England, A. F.; Ikariya, T.; Noyori, R. Angew. Chem., Int. Ed. 1998, 37, 1703-1707. (b) Ohkuma, T.; Ooka, H.; Yamakawa, M.; Ikariya, T.; Noyori, R. J. Org. Chem. 1996, 61, 4872-4873. (c) U.S. Pat. No. 5,856,590, 1999.
(8) (a) PCT Int. Appl. WO 02/22526 A2. (b) Abdur-Rashid, K.; Guo, R.; Lough, A. J.; Morris, R. H. Adv. Synth. Catal. 2005, 347, 571-579. (c) Guo, R.; Lough, A. J.; Morris, R. H.; Song, D. Organometallics 2004, 23, 5524-5529. (d) Guo, R.; Lough, A. J.; Morris, A. J.; Song, D. Organometallics 2005, 24 3354-3354.