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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D335-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D335-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-22
filingDate 1988-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1990-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_15aa1690501d6562f0f0735f828a3b68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8c6588c5c39f301306d9e5d1f2b23f5e
publicationDate 1990-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4918203-A
titleOfInvention Preparation of 6-substituted 4-chromanones
abstract Disclosed is a practical and efficient process for preparing 6-substituted 4-chromanones from phenolic acrylate ester compounds derivable from para-substituted phenolic or thiophenolic compounds and beta-unsubstituted acrylic acid compounds which are esterifiable therewith. The process includes effecting rearrangement of a phenolic or thiophenolic acrylate ester in the presence of a rearrangement effective amount of hydrogen fluoride to the corresponding hydroxy - or mercapto (vinyl ketone) wherein the carbonyl carbon atom of the vinyl carboxy group is directly attached to the benzene ring ortho to the hydroxy or mercapto group. Thereafter, the vinyl ketone is cyclized to the corresponding 6-substituted 4-chromanone in the presence of a cyclization-effective amount of hydrogen fluoride. The 6-substituted 4-chromanones prepared by the process are useful as intermediates for preparing pharmaceutical agents.
priorityDate 1985-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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