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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B57-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P41-003
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-44
filingDate 1991-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1992-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6e700d51b7965dc5edf205afd768441d
publicationDate 1992-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5126268-A
titleOfInvention Alcohol-ester sparation by reaction with acetate
abstract A process is disclosed for the isolation of an enantiomerically enriched alcohol from a first mixture of an enantiomerically enriched 1-arylsulfonate-2 -hydroxy-3-butene and an enantiomerically enriched 1 -arylsulfonate- 2-acyloxy-3-butene. The process includes the steps of: n (a) contacting the mixture with a reagent capable of reacting with said 1-arylsulfonate-2-hydroxy-3-butene to remove the arylsulfonate group and produce a mixture of dihydroxybutene monoesters thereby forming a second mixture containing said dihydroxybutene monoesters and unreacted enantiomerically enriched 1-arylsulfonate-2-acyloxy-3-butene n (b) contacting the second mixture with reagents capable of hydrolyzing all of the acyl groups in said mixture to hydroxy groups so as to produce a third mixture comprising 1,2-dihydroxy-3-butenes and enantiomerically enriched 1-arylsulfonate-2-hydroxy-3 -butene; n (c) washing said third mixture with water so as to remove said 1,2-dihydroxy-3-butenes.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101935239-B1
priorityDate 1990-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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