JPS54144332A - Racemization of optically active 2-(4-chlorophenyl)-3- methylbutyric acid - Google Patents

Racemization of optically active 2-(4-chlorophenyl)-3- methylbutyric acid

Info

Publication number
JPS54144332A
JPS54144332A JP5210178A JP5210178A JPS54144332A JP S54144332 A JPS54144332 A JP S54144332A JP 5210178 A JP5210178 A JP 5210178A JP 5210178 A JP5210178 A JP 5210178A JP S54144332 A JPS54144332 A JP S54144332A
Authority
JP
Japan
Prior art keywords
chlorophenyl
optically active
methylbutyric acid
racemization
carboxylic 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.)
Granted
Application number
JP5210178A
Other languages
English (en)
Other versions
JPS5748539B2 (ja
Inventor
Akio Higo
Yukio Suzuki
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP5210178A priority Critical patent/JPS54144332A/ja
Priority to EP79300717A priority patent/EP0006284B1/en
Priority to DE7979300717T priority patent/DE2960244D1/de
Priority to US06/034,696 priority patent/US4237313A/en
Publication of JPS54144332A publication Critical patent/JPS54144332A/ja
Publication of JPS5748539B2 publication Critical patent/JPS5748539B2/ja
Granted legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
    • C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to atoms of the carbocyclic ring
    • C07D317/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42—Separation; Purification; Stabilisation; Use of additives
    • C07C51/487—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to chemical modification

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
JP5210178A 1978-04-28 1978-04-28 Racemization of optically active 2-(4-chlorophenyl)-3- methylbutyric acid Granted JPS54144332A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP5210178A JPS54144332A (en) 1978-04-28 1978-04-28 Racemization of optically active 2-(4-chlorophenyl)-3- methylbutyric acid
EP79300717A EP0006284B1 (en) 1978-04-28 1979-04-27 Racemizing of optically active alpha-substituted-alpha-phenylacetic acids
DE7979300717T DE2960244D1 (en) 1978-04-28 1979-04-27 Racemizing of optically active alpha-substituted-alpha-phenylacetic acids
US06/034,696 US4237313A (en) 1978-04-28 1979-04-30 Racemization of optically active α-substituted-α-phenylacetic acid derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5210178A JPS54144332A (en) 1978-04-28 1978-04-28 Racemization of optically active 2-(4-chlorophenyl)-3- methylbutyric acid

Publications (2)

Publication Number Publication Date
JPS54144332A true JPS54144332A (en) 1979-11-10
JPS5748539B2 JPS5748539B2 (ja) 1982-10-16

Family

ID=12905446

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5210178A Granted JPS54144332A (en) 1978-04-28 1978-04-28 Racemization of optically active 2-(4-chlorophenyl)-3- methylbutyric acid

Country Status (4)

Country Link
US (1) US4237313A (ja)
EP (1) EP0006284B1 (ja)
JP (1) JPS54144332A (ja)
DE (1) DE2960244D1 (ja)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58174345A (ja) * 1982-04-06 1983-10-13 Sumitomo Chem Co Ltd 光学活性２，２−ジメチルシクロプロパン−１−カルボン酸ハライドのラセミ化方法
US4454344A (en) * 1982-08-23 1984-06-12 American Cyanamid Company Method for the resolution of racemic 2-(p-difluoromethoxyphenyl)-3-methylbutyric acid
US4506097A (en) * 1983-04-25 1985-03-19 American Cyanamid Co. Method for the racemization of (2)-2-(4-difluoromethoxyphenyl)-3-methylbutyric acid
US4613690A (en) * 1985-08-30 1986-09-23 Stauffer Chemical Company Racemization of optically active compounds having a bromine substituted chiral carbon atom
US6812363B2 (en) * 2002-10-15 2004-11-02 Usv Limited Racemization of optically active 2-substituted phenyl glycine esters
CN101628870B (zh) * 2009-09-08 2012-10-31 江苏耕耘化学有限公司 (R)-(-)-α-异丙基-4-氯苯乙酸二乙胺盐直接消旋化的方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH366842A (de) * 1958-05-20 1963-01-31 Inventa Ag Verfahren zur Racemisierung von optisch aktiven Aminosäuren
DE1445410A1 (de) * 1961-07-18 1969-04-10 Ajinomoto Kk Verfahren zur Racemisierung optisch aktiver Pyroglutaminsaeure
US3213106A (en) * 1961-11-16 1965-10-19 Ajinomoto Kk Process of racemizing optically active alpha acids
US3737454A (en) * 1969-09-10 1973-06-05 Tanabe Seiyaku Co Racemization of optically active ammonium n-acetyl-alpha-aminophenylacetate
JPS535134A (en) * 1976-06-30 1978-01-18 Sumitomo Chem Co Ltd Racemization of optical active 2-(4)chlorophenyl)-3-methylbutylic acid
JPS543035A (en) * 1977-06-09 1979-01-11 Sumitomo Chem Co Ltd Racemization of optical active 2-(4-chlorophenyl)-3-methyl-butyroyl chloride

Also Published As

Publication number Publication date
JPS5748539B2 (ja) 1982-10-16
EP0006284B1 (en) 1981-04-08
US4237313A (en) 1980-12-02
EP0006284A1 (en) 1980-01-09
DE2960244D1 (en) 1981-04-30

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