JPS6463539A - Optically active ethanol derivative and production thereof - Google Patents

Optically active ethanol derivative and production thereof

Info

Publication number
JPS6463539A
JPS6463539A JP9996188A JP9996188A JPS6463539A JP S6463539 A JPS6463539 A JP S6463539A JP 9996188 A JP9996188 A JP 9996188A JP 9996188 A JP9996188 A JP 9996188A JP S6463539 A JPS6463539 A JP S6463539A
Authority
JP
Japan
Prior art keywords
formula
optically active
halogen
liquid crystal
buffer solution
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
JP9996188A
Other languages
Japanese (ja)
Other versions
JP2689474B2 (en
Inventor
Takayuki Azumai
Masayoshi Minamii
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
Publication of JPS6463539A publication Critical patent/JPS6463539A/en
Application granted granted Critical
Publication of JP2689474B2 publication Critical patent/JP2689474B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

NEW MATERIAL:The optically active ethanol derivative of formula I (A is H, lower alkyl, lower alkoxy or halogen; Z is H or halogen; l is 0 or 1; *represents asymmetric C). EXAMPLE:(+)-4-Benzyloxy-1-phenethyl alcohol. USE:An intermediate for a liquid crystal material, especially a ferroelectric liquid crystal material having excellent stability and quick response and an intermediate for agricultural chemicals and pharmaceuticals, etc. PREPARATION:Ether one of optical active compounds of formula I can be produced by mixing (A) dl-esters of formula II (R' is lower alkyl) with (B) an esterase capable of hydrolyzing either one of the enantiomers of the above esters, e.g., an enzyme (such as lipase) originated from animals, vegetables or microorganisms, and vigorously agitating the mixture in a buffer solution (e.g. phosphate buffer solution) at 10-60 deg.C for 10-70hr to effect asymmetric hydrolysis. The unreacted ester is further hydrolyzed to obtain the other compound of formula I which is the antipod of the above compound.
JP63099961A 1987-04-30 1988-04-21 Optically active ethanol derivative and method for producing the same Expired - Lifetime JP2689474B2 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP10951187 1987-04-30
JP11198487 1987-05-07
JP62-109511 1987-05-07
JP62-111984 1987-05-07

Publications (2)

Publication Number Publication Date
JPS6463539A true JPS6463539A (en) 1989-03-09
JP2689474B2 JP2689474B2 (en) 1997-12-10

Family

ID=26449253

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63099961A Expired - Lifetime JP2689474B2 (en) 1987-04-30 1988-04-21 Optically active ethanol derivative and method for producing the same

Country Status (1)

Country Link
JP (1) JP2689474B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01104026A (en) * 1987-07-17 1989-04-21 Sumitomo Chem Co Ltd Optically active alcohols and their production
JPH02142746A (en) * 1988-11-24 1990-05-31 Arakawa Chem Ind Co Ltd Optically active compound and production thereof
JP2006248915A (en) * 2005-03-08 2006-09-21 Kyoto Univ Optically active sulfur-cross-linked binuclear ruthenium complex, method for producing the same, method for producing optically active compound using the same catalyst and new optically active compound

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
C R ACAD SC PARIS *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01104026A (en) * 1987-07-17 1989-04-21 Sumitomo Chem Co Ltd Optically active alcohols and their production
JPH02142746A (en) * 1988-11-24 1990-05-31 Arakawa Chem Ind Co Ltd Optically active compound and production thereof
JP2006248915A (en) * 2005-03-08 2006-09-21 Kyoto Univ Optically active sulfur-cross-linked binuclear ruthenium complex, method for producing the same, method for producing optically active compound using the same catalyst and new optically active compound

Also Published As

Publication number Publication date
JP2689474B2 (en) 1997-12-10

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