http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1206483-A

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N53-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-00
filingDate 1983-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1986-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de954b47a8a35d5bf6051f5e73614fff
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e831b1c44b585ea240625cbeb43a0ff
publicationDate 1986-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1206483-A
titleOfInvention Process for preparing cyclopropane carboxylic acid ester derivatives
abstract ABSTRACT PROCESS FOR PREPARING CYCLOPROPANE CARBOXYLIC ACID ESTER DERIVATIVES A process for preparing a compound according to formula I containing substantially equimolar amounts of the 1R cis S- and the 1S cis isomers (the cis-2 enantiomer pair) and substantially free of the 1R cis R- and the 1S cis S-isomers (the cis-1 enantiomer pair), (I) wherein R1 and R2 are each independently selected from chlorine, bromine and methyl, which process comprises contacting the cis-1 enantiomer pair, alone or in the presence of the cis-2 enantiomer pair, with an organic amine base containing from 5 to 7 carbon atoms and being a secondary amine containing two branched alkyl groups or being a tertiary amine, and then separating off a solid compound containing the cis-2 enantiomer pair and substantially free of the cis-1 enantiomer pair, characterized in that the reaction mixture is in the form a solid-liquid slurry.
priorityDate 1982-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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