http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9833787-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_70ec63d39d6704bacc5c7068c93ded43
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-89
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-567
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-567
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-89
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
filingDate 1998-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39667846b77b8663e6dff4adfd60c72a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0f55bf1c6d0260a90831e572422d9866
publicationDate 1998-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9833787-A1
titleOfInvention Process for the preparation of a carboxylic anhydride
abstract The present invention provides a colorless and transparent carboxylic anhydride with excellent stability in a liquid state at room temperature which is useful in uses such as a curing agent for epoxy resins, a liquid state encapsulant for semiconductors, and a liquid state encapsulant for light emission diodes. Said carboxylic anhydride which is a liquid at 20 °C containing a carboxylic anhydride not having carbon-carbon double bond such as 3-isobutyl-5,6-dimethylcyclohexane-1,2-dicarboxylic anhydride, 3-(β-methylbutyl)-5-methylcyclohexane-1,2-dicarboxylic anhydride, and 4-isohexylcyclohexane-1,2-dicarboxylic anhydride is prepared by forming an acid anhydride compound having a cyclohexane ring by a Diels-Alder reaction of a diene-hydrocarbon or triene-hydrocarbon having a carbon number of 10 with maleic anhydride, followed by carrying out a stereo-isomerization in the presence of a catalyst, and further carrying out hydrogenation of said reaction product.
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priorityDate 1997-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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