Patent Application
20050014959
The present invention relates to a process for preparing dihydroxycarboxylic esters and an overall process for preparing R-(+)-α-lipoic acid.
Dihydroxycarboxylic esters are valuable intermediates and synthesis building blocks in organic chemistry. In particular, (6S)-6,8-dihydroxyoctanoic esters serve as intermediates for the synthesis of enantiomerically pure R-(+)-α-lipoic acid.
EP 487 986 discloses preparing (6S)-6,8-dihydroxyoctanoic esters by reducing the corresponding (3S)-3-hydroxyoctanedioic diesters with complex hydrides in the presence of aprotic solvents.
Using this process, yields which are good but are still in need of improvement are achieved. In addition, the process has the disadvantages that relatively large amounts of complex hydrides must be used.
It is an object of the present invention, therefore, to provide a process for preparing dihydroxycarboxylic esters which does not have the disadvantages of the prior art and provides the dihydroxycarboxylic esters in improved yields.
We have found that this object is achieved by a process for preparing dihydroxycarboxylic esters of the formula I,
where
The index n which is the number of —CH2— radicals is 1, 2, 3, 4, 5, 6 or 7, preferably 3. In a preferred embodiment of the process, therefore dihydroxyoctanoic esters are prepared according to the invention.
The radicals R1 and R2 can be different or identical. The radicals R1 and R2 are therefore independently of one another an unsubstituted or substituted C1-C20-alkyl, preferably C1-C12-alkyl, particularly preferably C1-C4-alkyl, an unsubstituted or substituted C2-C20-alkenyl, preferably C2-C12-alkenyl, particularly preferably C1-C4-alkenyl, an unsubstituted or substituted C2-C20-alkynyl, preferably C2-C12-alkynyl, particularly preferably C1-C4-alkynyl, an unsubstituted or substituted C3-C8-cycloalkyl, an unsubstituted or substituted aralkyl, an unsubstituted or substituted aryl, an unsubstituted or substituted hydroxyalkyl or an unsubstituted or substituted hetaryl.
For all substituted radicals of the present invention, if the substituents are not specified in more detail, independently of one another there may be up to five substituents, for example selected from the following group:
A C2-C12-alkenyl radical for R1 and R2 is, independently of one another, for example, vinyl, 2-propenyl, 2-butenyl, 3-butenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-2-propenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1-ethyl-l-methyl-2-propenyl, 1-ethyl-2-methyl-2-propenyl and the corresponding heptenyls, octenyls, nonenyls, decenyls, undecenyls and dodecenyls.
A C2-C12-alkynyl radical for R1 and R2 is, independently of one another, for example, ethynyl, 2-propynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 1-methyl-2-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-4-pentynyl, 4-methyl-2-pentynyl, 1,1-dimethyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 1-ethyl-2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl and 1-ethyl-1-methyl-2-propynyl, preferably ethynyl, 2-propynyl, 2-butynyl, 1-methyl-2-propynyl or 1-methyl-2-butynyl, and the corresponding heptynyls, octynyls, nonynyls, decynyls, undecynyls and dodecynyls.
A C3-C8-cycloalkyl radical for R1 and R2 is, independently of one another, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl.
Preferred unsubstituted or substituted aryl radicals for R1 and R2 are, independently of one another, unsubstituted or substituted phenyl, 1-naphthyl or 2-naphthyl.
Preferred unsubstituted or substituted arylalkyl radicals for R1 and R2 are, independently of one another, unsubstituted or substituted benzyl or ethylenephenyl (homobenzyl).
Hetaryl radicals for R1 and R2 are, independently of one another, for example radicals such as 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-furyl, 3-furyl, 2-pyrrolyl, 3-pyrrolyl, 2-thienyl, 3-thienyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-pyrimidyl, 4-pyrimidyl, 5-pyrimidyl, 6-pyrimidyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 3-isothiazolyl, 4-isothiazolyl, 5-isothiazolyl, 2-imidazolyl, 4-imidazolyl, 5-imidazolyl, 3-pyridazinyl, 4-pyridazinyl, 5-pyridazinyl, 6-pyridazinyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, thiadiazolyl, oxadiazolyl or triazinyl.
Substituted hetaryl radicals R1 and R2 are, independently of one another, also anellated derivatives of the abovementioned hetaryl radicals, for example indazole, indole, benzothiophene, benzofuran, indoline, benzimidazole, benzthiazole, benzoxazole, quinoline, 2,3-dihydro-1-benzofuran, furo[2,3]pyridine, furo[3,2]pyridine or isoquinoline.
Hetarylalkyl radicals for R1 and R2 are, independently of one another, radicals which are composed, for example, of C1-C6-alkylene radicals and of the above-described hetaryl radicals, for example the radicals —CH2-2-pyridyl, —CH2-3-pyridyl, —CH2-4-pyridyl, —CH2-2-thienyl, —CH2-3-thienyl, —CH2-2-thiazolyl, —CH2-4-thiazolyl, CH2-5-thiazolyl, —CH2-CH2-2-pyridyl, —CH2-CH2-3-pyridyl, —CH2-CH2-4-pyridyl, —CH2-CH2-2-thienyl, —CH2-CH2-3-thienyl, —CH2-CH2-2-thiazolyl, —CH2-CH2-4-thiazolyl, or —CH2-CH2-5-thiazolyl.
Preferred radicals for R1 and R2 are, independently of one another, unsubstituted radicals. Particularly preferred radicals for R1 and R2 are, independently of one another, the above-described C1-C12-alkyl radicals, in particular C1-C4-alkyl, in particular methyl.
In a particularly preferred embodiment, the radicals R1 and R2 are identical.
The starting compounds of the inventive process are the hydroxycarboxylic diesters of the formula II. Preparation of these starting compounds is known per se and is described, for example, in EP 487 986 and in the references cited therein. Preferred hydroxycarboxylic diesters of the formula II as starting compounds are composed of the above-described preferred radicals R1 and R2 and the preferred index n.
Particularly preferred hydroxycarboxylic diesters of the formula II as starting compound are:
A particularly preferred starting compound is dimethyl (3S)-3-hydroxyoctanedioate.
Dihydroxycarboxylic esters of the formula I are prepared inventively as product compounds by reacting hydroxycarboxylic diesters of the formula II as starting compounds with complex hydrides and thus by reducing the hydroxycarboxylic diesters of the formula II as starting compounds in the presence of a solvent and in the presence of phase transfer catalysts.
Preferred complex hydrides are borohydrides, in particular ammonium borohydride, lithium borohydride, potassium borohydride and sodium borohydride, and also alkyl- and alkoxy-substituted borohydrides, for example lithium triethylborohydride and sodium trimethoxyborohydride. A particularly preferred complex hydride in the inventive process is sodium borohydride.
The molar ratio of complex hydrides to the hydroxycarboxylic diester of the formula II is not critical and is typically from 0.5:1 to 3:1, preferably from 0.5:1 to 1.5:1.
Preferred aprotic solvents are aliphatic and aromatic hydrocarbons, for example hexane, cyclohexane, toluene, benzene and xylene, and also ethers, for example dioxane, diethyl ether and tetrahydrofuran.
Particularly preferred aprotic solvents are aliphatic and aromatic hydrocarbons, for example hexane, cyclohexane, toluene, benzene and xylene, and very particularly preferred toluene.
Phase transfer catalysts are compounds which in a manner known per se are able to increase the exchange of compounds between at least two phases of the phase boundary, also termed the interphase. This can be a liquid/liquid or a liquid/solid phase boundary.
For the inventive process, in principle, all phase transfer catalysts are suitable.
Preference is given to phase transfer catalysts which are able to increase the exchange of compounds between an organic phase and an aqueous phase at the phase boundary. These phase transfer catalysts are described, for example, in E. V. Dehmlov, S. S. Dehmlov, Phase Transfer Catalysis, 3rd Edition, V C H Weinheim 1993, pages 65 to 71, in particular page 65.
Particularly preferred phase transfer catalysts are ammonium salts of the formula III
R3R4R5R6N+X− III
where
In a preferred embodiment, the phase transfer catalysts used are ammonium salts of the formula III.
The radicals R3, R4, R5 and R6 can be identical or different.
An aliphatic C1-C30-radical is preferably a C1-C30-alkyl, C2-C30-alkenyl, C2-C30-alkynyl or C3-C8-cycloalkyl radical.
Aralkyl or aryl radicals for R3, R4, R5 and R6 are preferably the corresponding radicals described above for R1 and R2.
The type of counterion X− is not critical; preferred counterions X− are halide, hydrogensulfate or hydroxide.
Particularly preferred phase transfer catalysts are tricaprylmethylammonium chloride which is commercially available as Aliquat 336(R), for example from Fluka or Adogen 464(R), for example from Aldrich, benzyltriethylammonium chloride or benzyltriethylammonium bromide, tetrabutylammonium chloride or tetrabutylammonium bromide or cetyltrimethylarmonium chloride or cetyltrimethylammonium bromide.
The amount of phase transfer catalyst is not critical and is typically from 0.1 to 20 mol %, based on the hydroxycarboxylic diester of the formula II.
The temperature at which the inventive process is carried out is not critical and is typically from 0 to 150° C., preferably from 20 to 110° C. The inventive process is typically carried out at atmospheric pressure, but can also be carried out at reduced or slightly elevated pressure, preferably at from 0.1 to 10 bar. The reaction times are not critical and are typically from 0.5 to 5 hours, in particular from 1 to 3 hours.
In order to speed up the process of the invention, it is advantageous to add catalytic amounts of methanol to the reaction mixture.
The dihydroxycarboxylic esters of the formula I are isolated in a manner known per se, for example, by working up the reaction mixture by hydrolysis, extraction and drying.
The inventive process has the advantage that the dihydroxycarboxylic esters of the formula I can be prepared in high yields and using relatively small amounts of complex hydrides.
The invention further relates to an overall process for preparing R-(+)-α-lipoic acid using the inventive process as an intermediate step.
The invention therefore relates to a process for preparing R-(+)-α-lipoic acid of the formula IV
which comprises preparing dihydroxycarboxylic esters of the formula I, where n is 3, by reacting the corresponding hydroxycarboxylic diesters of the formula II with complex hydrides in the presence of a solvent and in the presence of phase transfer catalysts and, in a manner known per se,
The examples below illustrate the invention.
2.68 g (70 mmol) of sodium borohydride were introduced together with 1.00 g (2.4 mmol) of Aliquat 336(R), from Avocado Research Chemicals, in 150 ml of toluene and 21.8 g (100 mmol) of dimethyl (3S)-3-hydroxyoctanedioate. The reaction mixture was stirred at approximately 75° C. until complete conversion (monitored by TLC).
After the batch cooled to room temperature, methanol was added, the mixture was acidified with methanolic hydrochloric acid and the solvent mixture was distilled off. After addition of further methanol, the distillation was repeated.
After removing traces of solvent in vacuo, 16.2 g of methyl (6S)-6,8-dihydroxyoctanoate were obtained. This corresponds to a yield of 85%.
2.68 g (70 mmol) of sodium borohydride were introduced in 150 ml of toluene and 21.8 g (100 mmol) of dimethyl (3S)-3-hydroxyoctanedioate were added. The reaction mixture was stirred at approximately 75° C. until complete conversion (monitoring by TLC).
After the batch cooled to room temperature, methanol was added, the mixture was acidified with methanolic hydrochloric acid and the solvent mixture was distilled off. After addition of further methanol, the distillation was repeated.
After removal of traces of solvent in vacuo, 7.6 g of methyl (6S)-6,8-dihydroxyoctanoate were obtained. This corresponds to a yield of 40%.
| Number | Date | Country | Kind |
|---|---|---|---|
| 101 60 148.4 | Dec 2001 | DE | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP02/13774 | 12/5/2002 | WO |
