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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D301-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D303-24
filingDate 2010-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_78f4cd259072f014a618288dd7782d4d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_16a4b6286c144527a334873a858b99af
publicationDate 2010-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2010275307-A
titleOfInvention Method for producing epoxy-terminated (meth) acrylate
abstract The present invention provides a production method for carrying out a transesterification reaction and further removing a metal alcoholate used as a transesterification catalyst by hydrolysis to obtain an epoxy group-terminated (meth) acrylate in a high yield. [MEANS FOR SOLVING PROBLEMS] A compound having a glycidyl group represented by the following general formula (2) and a (meth) acrylate compound, while removing the generated alcohol and solvent out of the reaction system by distillation in the presence of a metal alcoholate. A method for producing an epoxy group-terminated (meth) acrylate represented by the following general formula (1) by transesterification. [Selection figure] None
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2013053131-A
priorityDate 2009-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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