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filingDate 1978-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1980-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_59c0a3793976ffaf2676873afd5ac87e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e2e2c3d808e5442b98a6ade8e4a8799b
publicationDate 1980-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4233456-A
titleOfInvention Process for the manufacture of optically active, optionally substituted 2-amino-2-phenylacetic acid
abstract Optically active 2-amino-2-phenylacetic acid of the formula ##STR1## in which R 1 , R 2 and R 3 , which are identical or different, denote hydrogen, halogen, hydroxy, alkyl, acyl, or alkoxy, is prepared by asymmetrical transformation of a corresponding DL-aminophenylacetonitrile with L(+)-tartaric acid. To this end the corresponding DL-2-amino-2-phenyl-acetonitrile is reacted with approximately equimolar amounts of L(+)-tartaric acid in the presence of at least one alkanol having from 1 to 5 carbon atoms and/or at least one carbonyl compound at a temperature of from 0° to 50° C. and the mixture is stirred for 2 to 120 hours at the indicated temperature. The crystallized transformation product is separated, hydrolyzed by treatment with an acid and the desired product is isolated.
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