http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1182008-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d202e9e866984fe229f6facc38f1d740
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-395
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C59-68
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C59-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-395
filingDate 1967-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1eb582d942dfed8d7100c54fb72721f8
publicationDate 1970-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1182008-A
titleOfInvention Resolution of d1-(3-Trifluoromethylphenoxy)-(4-Chlorophenyl)Acetic Acid
abstract 1,182,008. Resolution of dl-(3-trifluoromethylphenoxy)(4-chlorophenyl) acetic acid. MERCK & CO. Inc. 27 Sept., 1967 [3 Oct., 1966], No. 44021/67. Heading C2C. Resolution of dl-(3-trifluoromethylphenoxy) (4-chlorophenyl) acetic acid is effected by treating the racemic acid with cinchonidine to form crystalline d-(3-trifluomethylphenoxy) (4-chlorophenyl) acetic acid cinchonidine salt, separating the salt from the liquor and treating the salt with acid to obtain pure disomer; allowing the liquor to stand for a protracted period to precipitate the l-acid isomer cinchonidine salt and treating the salt with acid to obtain l-isomer. The salts are preferably washed with a C 1-6 alkanol before treatment with the acid, e.g. H 2 SO 4 .
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priorityDate 1966-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Incoming Links

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Total number of triples: 34.