http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2020000359-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6486e2441acfcead84ce78a51bd8747b
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-66
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-66
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-65
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-618
filingDate 2018-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e5b54b9e0997df20288dd757abd1b4ac
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa9d974c87ed7c9af341aefe9c445a89
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f259f9a8b52c1baffd93164f9731ceee
publicationDate 2020-01-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2020000359-A1
titleOfInvention Method for preparing methyl benzoylcinnamate compound
abstract The present invention relates to a method for preparing a methyl benzoylcinnamate compound in formula (I), comprising: making a compound as shown in formula (II) contact with a compound as shown in formula (III) to perform an ester formation reaction to obtain the compound as shown in formula (I), wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, R12, R13, R14, and X are as defined in the description. According to the method of the present invention, the raw material for producing such photoinitiator is changed to an α-monohalogenoalkyl ketone compound from α-monohydroxyl ketone, so that production cost is lowered greatly, and the yield is increased evidently.
priorityDate 2018-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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