IP Library Granted Patent US 8,013,193
Granted Patent B2
US 8,013,193 · App. 12/594,577 · Granted Sep 6, 2011

Method for producing alcohol by hydrogenating lactone and carboxylic acid ester in liquid phase

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Quick Facts
Patent No.
US 8,013,193
App. No.
12/594,577
Granted
Sep 6, 2011
Kind
B2
Abstract

Disclosed is a method for producing an alcohol from a lactone or a carboxylic acid ester, which enables to produce an alcohol from a lactone or a carboxylic acid ester under relatively mild conditions with high yield and high catalytic efficiency. This method also enables to produce an optically active alcohol from an optically active lactone or an optically active carboxylic acid ester. Specifically disclosed is a method for producing an alcohol by hydrogen reducing a lactone or a carboxylic acid ester in the presence of a catalyst containing ruthenium and a phosphine compound represented by the following general formula (1): wherein R 1 represents a spacer; R 2 , R 3 , R 4 , R 5 , R 6 and R 7 independently represent a hydrogen atom, an alkyl group having 1-12 carbon atoms, an aryl group or a heterocyclic group; and R 8 , R 9 , R 10 , R 11 , R 12 and R 13 independently represent an alkyl group having 1-12 carbon atoms, an aryl group or a heterocyclic group.

Claims (19)

1. A method for producing an alcohol, comprising subjecting a lactone or a carboxylic acid ester to hydrogen reduction in a solvent or without solvent, in the presence of a catalyst containing ruthenium and a phosphine compound represented by the following formula (1):

wherein R 1 represents a spacer; R 2 , R 3 , R 4 , R 5 , R 6 and R 7 each independently represent a hydrogen atom, or an alkyl group having 1 to 12 carbon atoms, an aryl group or a heterocyclic group; and R 8 , R 9 , R 10 , R 11 , R 12 and R 13 each independently represent an alkyl group having 1 to 12 carbon atoms, an aryl group or a heterocyclic group.

2. The method for production according to claim 1 , wherein the lactone or carboxylic acid ester that is subjected to reduction is an optically active form, and the optical purity of the alcohol produced by the reduction retains an optical purity value of 90% or more of the value of the substrate that is subjected to reduction.

3. The method for production according to claim 1 , wherein the catalyst containing ruthenium and a phosphine compound is produced for immediate use.

4. The method for production according to claim 1 , wherein the catalyst containing ruthenium and a phosphine compound is a complex represented by the following formula (2):

[Ru 2 (μ−X 1 ) 3 (Phos) 2 ]X 2   (2)

wherein X 1 represents a halogen atom; X 2 represents a counter anion; and Phos represents the phosphine compound represented by the formula (1).

5. The method for production according to claim 1 , wherein the catalyst containing ruthenium and a phosphine compound is a complex represented by the following formula (3):

[Ru(Phos)(L 1 )(L 2 )(L 3 )](X 3 ) 2   (3)

wherein L 1 , L 2 and L 3 , which may be present singly or linked together, each represent a neutral ligand or a coordinating solvent; X 3 represents a counter anion; and Phos represents the phosphine compound represented by the formula (1).

6. The method for production according to claim 1 , wherein the catalyst containing ruthenium and a phosphine compound is a complex represented by the following formula (4):

[RuH(BH 4 )(Phos)]  (4)

wherein Phos represents the phosphine compound represented by the formula (1).

7. The method for production according to claim 1 , wherein the catalyst containing ruthenium and a phosphine compound is a complex represented by the following formula (5):

[Ru(H)(OAc)(Phos)]  (5)

wherein Ac represents an acetyl group; and Phos represents the phosphine compound represented by the formula (1).

8. The method for production according to claim 1 , wherein the solvent used in the hydrogenation reaction is an alcohol solvent.

9. The method for production according to claim 1 , wherein an additive is added to the reaction system.

10. The method for production according to claim 1 , wherein a reducing agent is added to the reaction system as a co-catalyst.

Assignments (2)
CHANGE OF ADDRESS Recorded Jan 15, 2014
From: KANEKA CORPORATION
To: KANEKA CORPORATION
Reel/Frame 032019/0901 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 2, 2009
From: MAEDA, HIROFUMI; INOUE, KENJI; MATSUMOTO, TAKAJI; NAGASAKI, IZURU; NOYORI, RYOJI; SAITO, SUSUMU
To: KANEKA CORPORATION; TAKASAGO INTERNATIONAL CORPORATION
Reel/Frame 023322/0764 →