WO2002030917A2 - Process for the production of racemic thioctic acid - Google Patents

Process for the production of racemic thioctic acid Download PDF

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Publication number
WO2002030917A2
WO2002030917A2 PCT/EP2001/011577 EP0111577W WO0230917A2 WO 2002030917 A2 WO2002030917 A2 WO 2002030917A2 EP 0111577 W EP0111577 W EP 0111577W WO 0230917 A2 WO0230917 A2 WO 0230917A2
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process according
group
halo
octanoic acid
esters
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PCT/EP2001/011577
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WO2002030917A3 (en
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Annibale Salvi
Stefano Maiorana
Francesco Corcella
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Laboratorio Chimico Internazionale SpA
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Laboratorio Chimico Internazionale SpA
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Priority to JP2002534303A priority Critical patent/JP4257572B2/en
Priority to EP01983530A priority patent/EP1330449B1/en
Priority to AT01983530T priority patent/ATE269319T1/en
Priority to US10/398,891 priority patent/US6844450B2/en
Priority to AU2002215012A priority patent/AU2002215012A1/en
Priority to KR1020037004735A priority patent/KR100822533B1/en
Priority to DE60103923T priority patent/DE60103923T2/en
Publication of WO2002030917A2 publication Critical patent/WO2002030917A2/en
Publication of WO2002030917A3 publication Critical patent/WO2002030917A3/en
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D339/00—Heterocyclic compounds containing rings having two sulfur atoms as the only ring hetero atoms
    • C07D339/02—Five-membered rings
    • C07D339/04—Five-membered rings having the hetero atoms in positions 1 and 2, e.g. lipoic acid

Definitions

  • the present invention relates to a process of synthesis of racemic thioctic acid with phase transfer catalysis. STATE OF THE ART
  • the state of the art describes processes of synthesis of racemic thioctic acid by reaction between sodium disuifide (Na 2 S 2 ), which is obtained in its turn from sulfur (S) and sodium sulfide (Na 2 S), and an alkyl ester of 6,8-dichlorooctanoic acid. Said processes are characterized by low yields (see J.A.C.S. Volume 79, 1957, page 6486). There was therefore the need to provide a process for the synthesis of racemic thioctic acid with high yield starting from the alkyl esters of 6,8- dichlorooctanoic acid.
  • An object of the present invention is therefore a process of synthesis of racemic thioctic acid comprising the following stages: a) reaction of the alkyl ester of 6,8-di-halo-octanoic acid in an organic solvent with an aqueous solution of alkali disuifide in presence of a compound for phase transfer catalysis selected from the group consisting of quaternary ammonium or phosphonium salts having the following general formula:
  • A is nitrogen of phosphorus
  • R-i is selected from the group consisting of Cl, Br, I, HSO 4 and H 2 P0 4 , and the substituents R-i, R 2) R 3 and R 4 are selected from the group consisting of linear or branched alkyl radicals having one to twenty carbon atoms (d-
  • the alkyl esters of 6,8-di-halo-octanoic acid are linear or branched C ⁇ -C 6 esters, and the halogen substituents, identical or different one from the other, are chosen from the group consisting of Cl, Br or I.
  • the alkyl esters of 6,8-di-halo-octanoic acid are preferably linear or branched C-i- C 3 esters, and the halogen substituents, identical or different one from the other, are Cl or Br.
  • the alkyl esters of 6,8-di-halo-octanoic acid are methyl ester br ethyl ester of 6,8-dichlorooctanoic acid.
  • the amount of alkyl esters of 6,8-di-halo- octanoic acid in the reaction taking place in stage a) is between 5 and 60% by weight, preferably between 10 and 40% by weight, still more preferably between 15 and 30% by weight with respect to the organic solvent.
  • the organic solvent used in the reaction taking place in stage a) is a solvent which cannot be mixed with water, selected from the group consisting of : linear or branched aliphatic C5-C10 hydrocarbons, or aromatic C 5 -C 10 hydrocarbons also having substituting groups selected from the group consisting of halogen, nitro or nitrile groups; esters of aliphatic or aromatic carboxylic acids; linear or cyclic ethers; linear or cyclic C4-C1 0 ketones, carbon disuifide, carbon tetrachloride.
  • the solvent is preferably benzene or toluene.
  • the process of synthesis of racemic thioctic acid according to present invention comprises the phase transfer of the disuifide ion from the aqueous solution containing the corresponding alkali disuifide to the organic phase which cannot be mixed with water, containing the alkyl ester of 6,8-di-halo-octanoic acid.
  • the aqueous solution of alkali disuifide can be prepared by reacting in water sulfur (S) with the corresponding alkali sulfide.
  • Preferred alkali disulfides are sodium disuifide (Na2S 2 ) and potassium disuifide (K 2 S 2 ) or their mixtures, still more preferred sodium disuifide.
  • the molar ratio alkali disulfide/alkyl ester.of 6,,8-di-halo-octanoic acid is between 0.8 and 1.2, preferably between 0.9 and 1.1 , still more preferably between 0.95 and 1.0.
  • the compounds for phase transfer catalysis used for the synthesis of thioctic acid which is the object of the present invention, are selected from the group consisting of tetrabutylammonium bromide, tetrabutylphosphonium bromide, methyltrioctylammonium chloride (ALIQUAT ® 336), methyl-(C ⁇ -C 10 )- trialkylammonium chloride (ADOGEN ® 464) and tetrabutylammonium hydrogensulfate; still more preferred are tetrabutylammonium bromide and tetrabutylammonium hydrogensulfate.
  • a quaternary salt in the reaction taking place in stage a) the compound for phase transfer catalysis, is present in an amount between 0.5 to 10% in moles, preferably between 1 to 5% in moles, still more preferably between 2 to 4% in moles with respect to the alkyl ester of 6,8-di-halo-octanoic acid.
  • the temperature of the reaction taking place in stage a) is between 20 and 130°C, preferably between 60 and 100°C, still more preferably between 80 and 90°C.
  • Stage b), i.e. hydrolysis of the ester of racemic thioctic acid is a hydrolysis with alkali/alkaline-earth hydroxides in presence of organic solvents, such as alcohols and polyols, ethers and hydroxy ethers, ketones and hydroxy ketones, which can be mixed with water in a volume ratio of 50:50 to 95:5 at a temperature between 0 and 100°C.
  • the concentration of the ester with respect to the organic solvent is between 5 and 50% w/v and the molar ratio ester/hydroxide is between 0.5 and 1.
  • Free racemic thioctic acid can be recovered by treatment with aqueous mineral acids diluted 1 to 20% by weight or water-soluble organic acids.
  • Reaction products and intermediate products are characterized with 1 H-NMR, Mass, HPLC analyses and potentiometric titration.
  • the following area some examples disclosing though not limiting the present invention.
  • Example 1- Synthesis of ethyl ester of racemic thioctic acid A mixture consisting of 16.91 g (0.13 moles) of sodium sulfide 60% by weight, 3.57 g (1.1 moles) of sulfur and 65 ml of water is heated at 85°C for 30 minutes. After being filtered to remove the insoluble portion, the solution is added in three hours to a solution consisting of 29.8 g (0.123 moles) of ethyl 6,8-dichlorooctanoate, 1.4 g (0.003 moles) of tetrabutylammonium bromide and 66 ml of toluene, kept at 82°C.
  • the organic phase is concentrated by solvent evaporation under vacuum and the residue obtained is cooled down at 0-5°C for 8-10 hours.
  • Said raw product is purified by dispersion under stirring in 6 ml of toluene and following crystallization from cyclohexane/ethyl acetate. 14.6 g of thioctic acid are obtained. The total yield is of 64%.
  • the thioctic acid obtained is thus characterized: melting point: 60-62°C titer > 99% (HPLC, potentiometric titration) HPLC purity > 99%

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)

Abstract

Process for the synthesis of racemic thiotic acid comprising the following stages: a) reaction of the alkyl ester of 6,8-di-halo-octanoic acid in an organic solvent with an aqueous solution of alkali disulfide in presence of a compound for phase transfer catalysis selected from the group consisting of quaternary ammonium or phosphonium salts having the following general formula: where: A is nitrogen of phosphorus, X is selected from the group consisting of Cl, Br, I, HSO4, and H2PO4 and the substitutents R1, R2, R3 and R4 are selection from the group consisting of linear or branched alkyl radicals having one to twenty carbon atoms (C1-C20), said substituents being identical or different one from the other, or only one of said substituents is selected from the group consisting of arylalkyl radicals having the following formula -(CH2)nC6H5 in which n=1-16; b) followed by the hydrolysis of the ester of racemic thiotic acid.

Description

PROCESS FOR THE PRODUCTION OF RACEMIC THIOCTIC ACID
FIELD OF THE INVENTION
The present invention relates to a process of synthesis of racemic thioctic acid with phase transfer catalysis. STATE OF THE ART
The state of the art describes processes of synthesis of racemic thioctic acid by reaction between sodium disuifide (Na2S2), which is obtained in its turn from sulfur (S) and sodium sulfide (Na2S), and an alkyl ester of 6,8-dichlorooctanoic acid. Said processes are characterized by low yields (see J.A.C.S. Volume 79, 1957, page 6486). There was therefore the need to provide a process for the synthesis of racemic thioctic acid with high yield starting from the alkyl esters of 6,8- dichlorooctanoic acid. SUMMARY It has now been found a new process of synthesis of racemic thioctic acid starting from the alkyl esters of 6,8-di-halo-octanoic acid, which can overcome the disadvantages characterizing the processes at the state of the art such as low yields and low quality.Quite unexpectedly and surprisingly, the Applicant has found a new process for the synthesis of racemic thioctic acid starting from the alkyl esters of 6,8-di-halo-octanoic acid, based on phase transfer catalysis, which allows to obtain a pure product with high yield. DETAILED DESCRIPTION OF THE INVENTION
An object of the present invention is therefore a process of synthesis of racemic thioctic acid comprising the following stages: a) reaction of the alkyl ester of 6,8-di-halo-octanoic acid in an organic solvent with an aqueous solution of alkali disuifide in presence of a compound for phase transfer catalysis selected from the group consisting of quaternary ammonium or phosphonium salts having the following general formula:
Figure imgf000002_0001
where:
A is nitrogen of phosphorus,
X is selected from the group consisting of Cl, Br, I, HSO4 and H2P04, and the substituents R-i, R2) R3 and R4 are selected from the group consisting of linear or branched alkyl radicals having one to twenty carbon atoms (d-
C20), said substituents being identical or different one from the other, or only one of said substituents is chosen from the group comprising arylalkyl radicals having the following formula -(CH2)nC6H5 in which n = 1-16; b) followed by the hydrolysis of the ester of racemic thioctic acid. According to the present invention the alkyl esters of 6,8-di-halo-octanoic acid are linear or branched Cι-C6 esters, and the halogen substituents, identical or different one from the other, are chosen from the group consisting of Cl, Br or I. The alkyl esters of 6,8-di-halo-octanoic acid are preferably linear or branched C-i- C3 esters, and the halogen substituents, identical or different one from the other, are Cl or Br.
Still more preferably, the alkyl esters of 6,8-di-halo-octanoic acid are methyl ester br ethyl ester of 6,8-dichlorooctanoic acid.
According to the present invention, the amount of alkyl esters of 6,8-di-halo- octanoic acid in the reaction taking place in stage a) is between 5 and 60% by weight, preferably between 10 and 40% by weight, still more preferably between 15 and 30% by weight with respect to the organic solvent.
The organic solvent used in the reaction taking place in stage a) is a solvent which cannot be mixed with water, selected from the group consisting of : linear or branched aliphatic C5-C10 hydrocarbons, or aromatic C5-C10 hydrocarbons also having substituting groups selected from the group consisting of halogen, nitro or nitrile groups; esters of aliphatic or aromatic carboxylic acids; linear or cyclic ethers; linear or cyclic C4-C10 ketones, carbon disuifide, carbon tetrachloride. The solvent is preferably benzene or toluene.
The process of synthesis of racemic thioctic acid according to present invention comprises the phase transfer of the disuifide ion from the aqueous solution containing the corresponding alkali disuifide to the organic phase which cannot be mixed with water, containing the alkyl ester of 6,8-di-halo-octanoic acid. The aqueous solution of alkali disuifide can be prepared by reacting in water sulfur (S) with the corresponding alkali sulfide.
Preferred alkali disulfides are sodium disuifide (Na2S2) and potassium disuifide (K2S2) or their mixtures, still more preferred sodium disuifide. In the reaction taking place in stage a) of the process of synthesis of racemic thioctic acid according to the present invention, the molar ratio alkali disulfide/alkyl ester.of 6,,8-di-halo-octanoic acid is between 0.8 and 1.2, preferably between 0.9 and 1.1 , still more preferably between 0.95 and 1.0. The compounds for phase transfer catalysis used for the synthesis of thioctic acid which is the object of the present invention, are selected from the group consisting of tetrabutylammonium bromide, tetrabutylphosphonium bromide, methyltrioctylammonium chloride (ALIQUAT® 336), methyl-(Cδ-C10)- trialkylammonium chloride (ADOGEN® 464) and tetrabutylammonium hydrogensulfate; still more preferred are tetrabutylammonium bromide and tetrabutylammonium hydrogensulfate.
According to the process of synthesis described in the present invention, in the reaction taking place in stage a) the compound for phase transfer catalysis, a quaternary salt, is present in an amount between 0.5 to 10% in moles, preferably between 1 to 5% in moles, still more preferably between 2 to 4% in moles with respect to the alkyl ester of 6,8-di-halo-octanoic acid.
The temperature of the reaction taking place in stage a) is between 20 and 130°C, preferably between 60 and 100°C, still more preferably between 80 and 90°C. Stage b), i.e. hydrolysis of the ester of racemic thioctic acid is a hydrolysis with alkali/alkaline-earth hydroxides in presence of organic solvents, such as alcohols and polyols, ethers and hydroxy ethers, ketones and hydroxy ketones, which can be mixed with water in a volume ratio of 50:50 to 95:5 at a temperature between 0 and 100°C. The concentration of the ester with respect to the organic solvent is between 5 and 50% w/v and the molar ratio ester/hydroxide is between 0.5 and 1. Free racemic thioctic acid can be recovered by treatment with aqueous mineral acids diluted 1 to 20% by weight or water-soluble organic acids.
Reaction products and intermediate products are characterized with 1H-NMR, Mass, HPLC analyses and potentiometric titration. The following area some examples disclosing though not limiting the present invention.
Example 1- Synthesis of ethyl ester of racemic thioctic acid A mixture consisting of 16.91 g (0.13 moles) of sodium sulfide 60% by weight, 3.57 g (1.1 moles) of sulfur and 65 ml of water is heated at 85°C for 30 minutes. After being filtered to remove the insoluble portion, the solution is added in three hours to a solution consisting of 29.8 g (0.123 moles) of ethyl 6,8-dichlorooctanoate, 1.4 g (0.003 moles) of tetrabutylammonium bromide and 66 ml of toluene, kept at 82°C. The mixture is refluxed (90°C) for 1 hour and cooled down at 30°C, the organic phase is separated and washed with 13 ml of water. The whole is concentrated under vacuum, thus obtaining 25.8 g of ethyl ester of thioctic acid (yield = 90%). The final product is characterized by means of 1H-NMR and Mass analyses:
• 1H-NMR - δ (300 MHz, CDCI3) : 1.2 (3H,t); 1.4 (2H,m); 1.65 (4H,m); 1.85 (1 H, td); 2.25 (2H, t); 2.4 (1 H, td); 3.1 (2H,m); 3.5 (1 H,m); 4.1 (2H,q).
• Mass (El) : 234 (M+); 189 (-CH3CH20). Example 2 - Hydrolysis of ester of thioctic acid
25.8 g (0.11 moles) of ethyl ester of thioctic acid are added to a solution consisting of 9.88 g (0.152 moles) of potassium hydroxide at 90% by weight, 74 ml of methanol and 13.5 ml of water. The mixture obtained is heated at 50°C for 2 hours and cooled down at 30°C, then 220 ml of toluene are added. The whole is acidified with phosphoric acid 10% by weight, keeping temperature between 30 and 40°C. The organic phase is separated and washed three times, each time with 50 ml of an aqueous solution of sodium chloride at 10% by weight. The organic phase is concentrated by solvent evaporation under vacuum and the residue obtained is cooled down at 0-5°C for 8-10 hours. The wax-like solid is filtered, thus obtaining 18.2 g of raw thioctic acid (yield = 80.3%). Said raw product is purified by dispersion under stirring in 6 ml of toluene and following crystallization from cyclohexane/ethyl acetate. 14.6 g of thioctic acid are obtained. The total yield is of 64%.
The thioctic acid obtained is thus characterized: melting point: 60-62°C titer > 99% (HPLC, potentiometric titration) HPLC purity > 99%

Claims

1. Process for the synthesis of racemic thioctic acid comprising the following stages: a) reaction of the alkyl ester of 6,8-di-halo-octanoic acid in an organic solvent with an aqueous solution of alkali disuifide in presence of a compound for phase transfer catalysis-selected from the group consisting of quaternary ammonium or phosphonium salts having the following general formula:
Figure imgf000007_0001
where:
A is nitrogen of phosphorus, X is selected from the group consisting of Cl, Br, I, HS04 and H2PO4 and the substituents Rι, R2, R3 and R are selected from the group consisting linear or branched alkyl radicals having one to twenty carbon atoms {C1-C20), said substituents being identical or different one from the other, or only one of said substituents is selected from the group consisting of arylalkyl radicals having the following formula -(CH2)nC6H5 in which n = 1 -16; b) followed by the hydrolysis of the ester of racemic thioctic acid.
2. Process according to claim 1 , wherein the alkyl esters of 6,8-di-halo-octanoic acid are linear or branched C-i-Cβ esters, and the halogen substituents, identical or different one from the other, are selected from the group consisting of Cl, Br or I.
3. Process according to claim 2, wherein said alkyl esters of 6,8-di-halo-octanoic acid are linear or branched C1-C3 esters, and the halogen substituents, identical or different one from the other, are Cl or Br.
4. Process according to claim 3, wherein said alkyl esters of 6,8-di-halo-octanoic acid are methyl ester or ethyl ester of 6,8-dichlorooctanoic acid.
5. Process according to claim 1 , wherein the amount of alkyl esters of 6,8-di-halo- octanoic acid in the reaction taking place in stage a) is between 5 and 60% by weight with respect to the organic solvent.
6. Process according to claim 5, wherein the amount of said esters is between 10 and 40% by weight with respect to the organic solvent.
7. Process according to claim 6, wherein the amount of said esters is between 15 and 30% by weight with respect to the organic solvent.
8. Process according to claim 1 , wherein the organic solvent used in the reaction taking place in stage a) is a solvent which cannot be mixed with water, selected from the group consisting of : linear or branched aliphatic C5-C10 hydrocarbons, or aromatic C5-C10 hydrocarbons also having substituting groups selected from the group consisting of halogen, nitro or nitrile groups; esters of aliphatic or aromatic carboxylic acids; linear or cyclic ethers; linear or cyclic C4-C10 ketones; carbon disuifide; carbon tetrachloride.
9. Process according to claim 8, wherein said solvent is benzene or toluene.
10. Process according to claim 1 , wherein the alkali disulfides are sodium disuifide (Na2S2) or potassium disulfide(K2S2) or their mixture.
11. Process according to claim 10, wherein said alkali disuifide is sodium disuifide.
12. Process according to claim 1 , wherein in the reaction taking place in stage a) the molar ratio alkali disulfide/alkyl ester of 6,8-di-halo-octanoic acid is between
0.8 and 1.2.
13. Process according to claim 12, wherein said molar ratio is between 0.9 and
1.1.
14. Process according to claim 13, wherein said molar ratio is between 0.95 and 1.0.
15. Process according to claim 1 , wherein the quaternary ammonium or phosphonium salts are selected from the group consisting of tetrabutylammonium bromide, tetrabutylphosphonium bromide, methyltrioctylammonium chloride (ALIQUAT® 336), methyl-(C8-Cι0)-trialkylammonium chloride (ADOGEN® 464) and tetrabutylammonium hydrogensulfate.
16. Process according to claim 15, wherein said quaternary salts are tetrabutylammonium bromide or tetrabutylammonium hydrogensulfate.
17. Process according to claim 1 , wherein said quaternary ammonium or phosphonium salt is present in an amount. of 0.5 to 10% in moles with respect to the alkyl ester of 6,8-di-halo-octanoic acid.
18. Process according to claim 17, wherein said quaternary salt is present in an amount of 1 to 5% in moles with respect to the alkyl ester of 6,8-di-halo-octanoic acid.
19. Process according to claim 18, wherein said quaternary salt is present in an amount of 2 to 4% in moles with respect to the alkyl ester of 6,8-di-halo-octanoic acid.
20. Process according to claim 1 , wherein the temperature of the reaction taking place in stage a) is between 20 and 130°C.
21. Process according to claim 20, wherein said temperature is between 60 and 100°C.
22. Process according to claim 21 , wherein said temperature is between 80 and 90°C.
PCT/EP2001/011577 2000-10-10 2001-10-08 Process for the production of racemic thioctic acid Ceased WO2002030917A2 (en)

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JP2002534303A JP4257572B2 (en) 2000-10-10 2001-10-08 Method for producing racemic thioctic acid
EP01983530A EP1330449B1 (en) 2000-10-10 2001-10-08 Process for the production of racemic thioctic acid
AT01983530T ATE269319T1 (en) 2000-10-10 2001-10-08 METHOD FOR PRODUCING RACEMIC THIOCTIC ACID
US10/398,891 US6844450B2 (en) 2000-10-10 2001-10-08 Process for the production of a racemic thioctic acid
AU2002215012A AU2002215012A1 (en) 2000-10-10 2001-10-08 Process for the production of racemic thioctic acid
KR1020037004735A KR100822533B1 (en) 2000-10-10 2001-10-08 Method for producing racemic thioctic acid
DE60103923T DE60103923T2 (en) 2000-10-10 2001-10-08 PROCESS FOR THE PREPARATION OF RAZEMIC THIOCTIC ACID

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ITMI2000A002186 2000-10-10
IT2000MI002186A IT1319194B1 (en) 2000-10-10 2000-10-10 RACEMO TIOTIC ACID PRODUCTION PROCESS.

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7235582B2 (en) 2003-04-22 2007-06-26 Laboratorio Chimico Internazionale S.P.A. Basic salt of thioctic acid with L-carnitine
WO2007138022A2 (en) 2006-05-25 2007-12-06 Eurand Pharmaceuticals Limited Lipoic acid pellets
CN102558142A (en) * 2010-12-23 2012-07-11 重庆药友制药有限责任公司 Preparation method of alpha-lipoic acid bulk pharmaceutical
CN112574171A (en) * 2020-12-15 2021-03-30 南京新百药业有限公司 Preparation method of lipoic acid
CN116135849A (en) * 2023-03-02 2023-05-19 厦门金达威维生素有限公司 A kind of synthetic method of lipoic acid

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10137381A1 (en) * 2001-07-31 2003-02-13 Viatris Gmbh New crystalline modifications of R-thioctic acid trometamol salt, useful as antiinflammatory agent, for treating diabetes mellitus or as appetite suppressant
DE10201464B4 (en) * 2002-01-16 2005-06-16 Viatris Gmbh & Co. Kg Process for the preparation of pure thioctic acid
CN106349323B (en) * 2016-08-25 2018-04-10 桂林益天成生物科技有限公司 The method that hydrolysis asiatic centella total saponins prepare asiaticoside member
CN108774209A (en) * 2018-08-03 2018-11-09 苏州富士莱医药股份有限公司 A method of lipoic acid ethyl ester is prepared using tubular reactor
CN116969917B (en) * 2023-05-30 2025-12-23 风火轮(上海)生物科技有限公司 Method for synthesizing lipoic acid ester by utilizing buffer salt

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA608575A (en) * 1960-11-15 S. Acker Donald Preparation of lipoic acid
US2792406A (en) 1954-06-01 1957-05-14 Du Pont Process of preparing alpha-lipoic acid using dichlorooctanoate and metal disulfide
DE3814163A1 (en) * 1988-04-27 1989-11-09 Rhein Chemie Rheinau Gmbh METHOD FOR PRODUCING DISULFIDES
DE4342619A1 (en) * 1993-12-14 1995-06-22 Bayer Ag Improved process for the preparation of 2,2'-dinitrodiphenyl disulfide
GB9510858D0 (en) 1995-05-30 1995-07-26 Chiroscience Ltd Process for preparing lipoic acid
DE19533881A1 (en) * 1995-09-13 1997-03-20 Dresden Arzneimittel Production and use of the pure enantiomers of 8-chloro-6-sulfonyloxy-octanoic acids and their alkyl esters and of the pure enantiomers of 6,8-dichloro-octanoic acid and their alkyl esters

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7235582B2 (en) 2003-04-22 2007-06-26 Laboratorio Chimico Internazionale S.P.A. Basic salt of thioctic acid with L-carnitine
WO2007138022A2 (en) 2006-05-25 2007-12-06 Eurand Pharmaceuticals Limited Lipoic acid pellets
CN102558142A (en) * 2010-12-23 2012-07-11 重庆药友制药有限责任公司 Preparation method of alpha-lipoic acid bulk pharmaceutical
CN112574171A (en) * 2020-12-15 2021-03-30 南京新百药业有限公司 Preparation method of lipoic acid
CN116135849A (en) * 2023-03-02 2023-05-19 厦门金达威维生素有限公司 A kind of synthetic method of lipoic acid

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US20040030157A1 (en) 2004-02-12
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WO2002030917A3 (en) 2002-07-25
ITMI20002186A1 (en) 2002-04-10
ATE269319T1 (en) 2004-07-15
EP1330449A2 (en) 2003-07-30
DE60103923T2 (en) 2005-06-30
DE60103923D1 (en) 2004-07-22
JP2004511475A (en) 2004-04-15
JP4257572B2 (en) 2009-04-22
EP1330449B1 (en) 2004-06-16
ES2222399T3 (en) 2005-02-01
KR100822533B1 (en) 2008-04-16

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