JPH1175889A5 - - Google Patents

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Publication number
JPH1175889A5
JPH1175889A5 JP1998151307A JP15130798A JPH1175889A5 JP H1175889 A5 JPH1175889 A5 JP H1175889A5 JP 1998151307 A JP1998151307 A JP 1998151307A JP 15130798 A JP15130798 A JP 15130798A JP H1175889 A5 JPH1175889 A5 JP H1175889A5
Authority
JP
Japan
Prior art keywords
optically active
lactic acid
trifluoromethyl lactic
bacterial cell
trifluoromethyl
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.)
Pending
Application number
JP1998151307A
Other languages
Japanese (ja)
Other versions
JPH1175889A (en
Filing date
Publication date
Application filed filed Critical
Priority to JP15130798A priority Critical patent/JPH1175889A/en
Priority claimed from JP15130798A external-priority patent/JPH1175889A/en
Priority to PCT/JP1998/003160 priority patent/WO1999004028A1/en
Publication of JPH1175889A publication Critical patent/JPH1175889A/en
Publication of JPH1175889A5 publication Critical patent/JPH1175889A5/ja
Pending legal-status Critical Current

Links

Description

(式中、Rは置換又は非置換の炭素原子数1〜12の炭化水素基である。)で表されるラセミ体α−トリフルオロメチル乳酸エステルを、エステル不斉加水分解能力を有する酵素、酵素固定化物、微生物、菌体培養液、又は菌体処理物の存在下で不斉加水分解させ、得られる光学活性α−トリフルオロメチル乳酸又はその未反応対掌体エステルを加水分解して得られる対掌体光学活性α−トリフルオロメチル乳酸を晶析する光学活性α−トリフルオロメチル乳酸の製造方法。
(2)上記(1)記載の方法で得られる光学活性α−トリフルオロメチル乳酸を再結晶し、結晶を回収する光学活性α−トリフルオロメチル乳酸の製造方法。
(wherein R is a substituted or unsubstituted hydrocarbon group having 1 to 12 carbon atoms), in the presence of an enzyme, an immobilized enzyme, a microorganism, a bacterial cell culture solution, or a treated bacterial cell product having the ability to asymmetrically hydrolyze esters, and then hydrolyzing the resulting optically active α-trifluoromethyllactic acid or its unreacted enantiomer ester to crystallize the enantiomer, optically active α-trifluoromethyllactic acid.
(2) A method for producing optically active α-trifluoromethyl lactic acid, which comprises recrystallizing the optically active α-trifluoromethyl lactic acid obtained by the method described in (1) above and recovering the crystals.

Claims (2)

一般式(I):
(式中、Rは置換又は非置換の炭素原子数1〜12の炭化水素基である。)
で表されるラセミ体α−トリフルオロメチル乳酸エステルを、エステル不斉加水分解能力を有する酵素、酵素固定化物、微生物、菌体培養液、又は菌体処理物の存在下で不斉加水分解させ、得られる光学活性α−トリフルオロメチル乳酸又はその未反応対掌体エステルを加水分解して得られる対掌体光学活性α−トリフルオロメチル乳酸を晶析する光学活性α−トリフルオロメチル乳酸の製造方法。
General formula (I):
(wherein R is a substituted or unsubstituted hydrocarbon group having 1 to 12 carbon atoms).
in the presence of an enzyme, an immobilized enzyme, a microorganism, a bacterial cell culture solution, or a treated bacterial cell product, which has the ability to asymmetrically hydrolyze an ester, and then the obtained optically active α-trifluoromethyl lactic acid or its unreacted enantiomer ester is hydrolyzed to crystallize the enantiomer, optically active α-trifluoromethyl lactic acid.
請求項1記載の方法で得られる光学活性α−トリフルオロメチル乳酸を再結晶し、結晶を回収する光学活性α−トリフルオロメチル乳酸の製造方法。A method for producing optically active α-trifluoromethyl lactic acid, which comprises recrystallizing the optically active α-trifluoromethyl lactic acid obtained by the method of claim 1 and recovering the crystals.
JP15130798A 1997-07-15 1998-06-01 Production method and purification method of optically active α-trifluoromethyl lactic acid and its enantiomer ester Pending JPH1175889A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP15130798A JPH1175889A (en) 1997-07-15 1998-06-01 Production method and purification method of optically active α-trifluoromethyl lactic acid and its enantiomer ester
PCT/JP1998/003160 WO1999004028A1 (en) 1997-07-15 1998-07-14 PROCESS FOR PREPARING OPTICALLY ACTIVE α-TRIFLUOROMETHYLLACTIC ACID AND ANTIPODE ESTERS THEREOF AND METHOD OF PURIFICATION THEREOF

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP9-189525 1997-07-15
JP18952597 1997-07-15
JP15130798A JPH1175889A (en) 1997-07-15 1998-06-01 Production method and purification method of optically active α-trifluoromethyl lactic acid and its enantiomer ester

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2007061892A Division JP2007202563A (en) 1997-07-15 2007-03-12 Method for producing and purifying optically active α-trifluoromethyl lactic acid and its enantiomer ester

Publications (2)

Publication Number Publication Date
JPH1175889A JPH1175889A (en) 1999-03-23
JPH1175889A5 true JPH1175889A5 (en) 2005-09-29

Family

ID=26480602

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15130798A Pending JPH1175889A (en) 1997-07-15 1998-06-01 Production method and purification method of optically active α-trifluoromethyl lactic acid and its enantiomer ester

Country Status (2)

Country Link
JP (1) JPH1175889A (en)
WO (1) WO1999004028A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1155138B1 (en) * 1999-02-23 2005-01-05 Lonza AG Method for preparing optically active 3,3,3-trifluoromethyl-2-alkyl propionic acid derivatives
JP4711367B2 (en) * 2000-09-20 2011-06-29 三菱レイヨン株式会社 Method for producing optically active amino alcohol derivative
JP4775925B2 (en) * 2001-09-10 2011-09-21 三菱レイヨン株式会社 Process for producing optically active α-trifluoromethyl lactic acid
MX2009011253A (en) * 2007-04-18 2009-12-02 Intendis Gmbh Process for the manufacture for non-steroidal anti-inflammatory agents and intermediates thereof.

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0578277A (en) * 1991-03-04 1993-03-30 Nikko Kyodo Co Ltd Production of 3,3,3-trifluorolactic acid and method for improving optical purity
GB9607458D0 (en) * 1996-04-10 1996-06-12 Zeneca Ltd Enzymatic process for stereoselective preparation of therapeutic amides

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