ES2117289T3 - Procedimiento para la obtencion del acido (l)-2-cloropropionico y sus sales. - Google Patents

Procedimiento para la obtencion del acido (l)-2-cloropropionico y sus sales.

Info

Publication number
ES2117289T3
ES2117289T3 ES94925459T ES94925459T ES2117289T3 ES 2117289 T3 ES2117289 T3 ES 2117289T3 ES 94925459 T ES94925459 T ES 94925459T ES 94925459 T ES94925459 T ES 94925459T ES 2117289 T3 ES2117289 T3 ES 2117289T3
Authority
ES
Spain
Prior art keywords
pct
chloropropionic
sec
optically active
acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
ES94925459T
Other languages
English (en)
Inventor
Wolfgang Ladner
Hansjorg Rettenmaier
Bernhard Zipperer
Hanspeter Hansen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Application granted granted Critical
Publication of ES2117289T3 publication Critical patent/ES2117289T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/005—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of carboxylic acid groups in the enantiomers or the inverse reaction
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/09—Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid esters or lactones
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Microbiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

SE DESCRIBE UNA PROCESO PARA LA PREPARACION DE ACIDO (L)-2CLOROPROPIONICO Y SUS SALES DE METAL ALCALINO, METAL ALCALINOTERRERO O SALES DE AMONIO. PARA ESTE OBJETIVO, EL ESTER ISOBUTILO DE ACIDO L-CLOROPROPIONICO ES HIDROLIZADO EN UN PH DESDE 4 HASTA 8 EN PRESENCIA DE UNA LIPASA A PARTIR DE PSEUDOMONAS DE ESPECIFICACION DSM 8246 Y EL PRODUCTO DE REACCION ACTIVO OPTICAMENTE SE AISLA A PARTIR DE LA MEZCLA DE REACCION O REACCIONA POSTERIORMENTE IN SITU EN UNA MANERA CONOCIDA POR SI MISMA, BIEN DIRECTAMENTE O DESPUES DE CONVERSION DE LA SAL EN EL ACIDO. LOS PRODUCTOS ACTIVOS OPTICAMENTE OBTENIDOS MEDIANTE ESTE PROCESO CONSTITUYEN PRODUCTOS INTERMEDIOS IMPORTANTES PARA LA PREPARACION DE AGENTES PROTECTORES DE PLANTAS.
ES94925459T 1993-08-23 1994-08-17 Procedimiento para la obtencion del acido (l)-2-cloropropionico y sus sales. Expired - Lifetime ES2117289T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE4328231A DE4328231C1 (de) 1993-08-23 1993-08-23 Verfahren zur Herstellung von (L)-2-Chlorpropionsäure und deren Salzen

Publications (1)

Publication Number Publication Date
ES2117289T3 true ES2117289T3 (es) 1998-08-01

Family

ID=6495763

Family Applications (1)

Application Number Title Priority Date Filing Date
ES94925459T Expired - Lifetime ES2117289T3 (es) 1993-08-23 1994-08-17 Procedimiento para la obtencion del acido (l)-2-cloropropionico y sus sales.

Country Status (9)

Country Link
US (1) US5753495A (es)
EP (1) EP0714447B1 (es)
JP (1) JPH09501570A (es)
AT (1) ATE166393T1 (es)
CA (1) CA2169659A1 (es)
DE (2) DE4328231C1 (es)
DK (1) DK0714447T3 (es)
ES (1) ES2117289T3 (es)
WO (1) WO1995006130A1 (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100613691B1 (ko) * 2004-09-07 2006-08-21 한국화학연구원 토양 메타게놈 유래 신규 리파제 및 이를 이용하여 라세믹에틸 2-브로모프로피오네이트를 선택적으로 분할하는 방법
CN100436399C (zh) * 2006-06-27 2008-11-26 浙江工业大学 一种制备(s)-(-)-2-氯丙酸酯和(r)-(+)-2-氯丙酸的方法
CN105732358A (zh) * 2016-04-06 2016-07-06 衢州信步化工科技有限公司 一种l-2-氯丙酸钠的合成方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5794295A (en) * 1980-12-04 1982-06-11 Sagami Chem Res Center Preparation of optically active ester and/or acid
JPS61111699A (ja) * 1984-11-02 1986-05-29 Toray Ind Inc 光学活性α−クロロプロピオン酸の製造法
US4668628A (en) * 1985-04-01 1987-05-26 Stauffer Chemical Company Resolution of racemic mixtures of aliphatic acid esters
JPS62205797A (ja) * 1986-03-05 1987-09-10 Daicel Chem Ind Ltd 光学活性化合物の製造法
JPS6352896A (ja) * 1986-08-22 1988-03-07 ストウフア−　ケミカル　カンパニ− リパ−ゼ酵素反応の実施方法
AT398081B (de) * 1991-04-29 1994-09-26 Chemie Linz Gmbh Verfahren zur enzymatischen hydrolyse eines carbonsäurederivates

Also Published As

Publication number Publication date
WO1995006130A1 (de) 1995-03-02
JPH09501570A (ja) 1997-02-18
EP0714447B1 (de) 1998-05-20
DE4328231C1 (de) 1994-07-28
DK0714447T3 (da) 1998-10-07
DE59406040D1 (de) 1998-06-25
US5753495A (en) 1998-05-19
ATE166393T1 (de) 1998-06-15
CA2169659A1 (en) 1995-03-02
EP0714447A1 (de) 1996-06-05

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