http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5528939-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H01M8-222
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H01M8-04186
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01M8-22
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01M8-04
filingDate 1978-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6ca7812df3e9833a2e81b1908e90902b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d58d0b448f00eb33e7b7b300c45839a
publicationDate 1980-02-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5528939-A
titleOfInvention Preparation of alpha-(2-hydroxyalkylamino)-epsilon-caprolactam
abstract PURPOSE: To obtain the title compound useful as raw materials for polymers, curing accelerators for epoxy resins, pesticides, and their intermediates, in a high selectivity, by reacting the amino group of α-amino-ε-caprolactam with an epoxy compound readily. n CONSTITUTION: α-Amino-ε-caprolactam, obtained by amination of α-chloro-ε-capolactam, is reacted with an epoxy compound of formula I: [R 1 is H, lower alkyl, lower halogenated alkyl, methylol, or group formula IV(R 2 is H, alkyl, acrylate, or methacrylate group)], e.g. ethylene oxide, in a solvent, e.g. water or chloroform, at 20W150°C to give the title compound of formula II: (R 4 is formula III; R 3 is H or formula III). n COPYRIGHT: (C)1980,JPO&Japio
priorityDate 1978-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 31.