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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B57-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D223-12
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filingDate 1985-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df61604caeffbfa70975c29268101185
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d05f21d8da59e7a04d37cfacbed44e63
publicationDate 1987-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S62114969-A
titleOfInvention Production of optically active alpha-amino-epsilon-caprolactam
abstract PURPOSE: To obtain the titled compound in high yield and optical purity with simple procedure, by carrying out the optical resolution of DL-α-amino-ε- caprolactam using an optically active N-benzoyl-methionine as an optical resolution agent. n CONSTITUTION: 1mol of DL-α-amino-ε-caprolactam (abbreviated as DL-ACL) is made to contact with 0.1W2.0mol of N-benzoyl-L-methionine and N-benzoyl-D- methionine used as an optical resolution agent at 0W80°C preferably in water. A hardly soluble diastereomer salt is crystallized from the resultant solution e.g. by cooling the solution. The salt is separated by a solid-liquid separation process such as filtration, centrifugal separation, etc., and is subjected to optical resolution e.g. by contacting with a cation exchange resin in an aqueous solvent. The resolution agent is separated and the cation exchange resin is eluted with NH 3 , etc., to obtain D-ACL or L-ACL. n USE: Intermediate for L-lysine or raw material of pharmaceuticals such as hypotensor. n COPYRIGHT: (C)1987,JPO&Japio
priorityDate 1985-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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