http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2000247948-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D201-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D223-10
filingDate 1999-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_719b9499e69b3427d8cc79d865715645
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4d38943ba4579db0403196f008afbeb9
publicationDate 2000-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2000247948-A
titleOfInvention Method for purifying ε-caprolactam and method for producing ε-caprolactam
abstract PROBLEM TO BE SOLVED: To provide high-concentration cyclohexanone oxime, 1,2,3,4,6,7,8,9-octahydrophenazine, 3-N-methyl-4,5,6,7 as impurities -To provide a process for producing ε-caprolactam, which can economically remove these impurities to a high degree from crude ε-caprolactam containing tetrahydrobenzimidazole and caprenolactams. SOLUTION: A crude ε-caprolactam is crystallized using a hydrocarbon-based solvent, and then brought into contact with hydrogen in the presence of a hydrogenation catalyst to produce ε-caprolactam.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014139152-A
priorityDate 1998-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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