http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1146952-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_00c9d781df3d4457e18aaf9b2ca26d06
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-16
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-04
filingDate 1980-02-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1983-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_702c70250aeab9423d7b664d590fa292
publicationDate 1983-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1146952-A
titleOfInvention Process for making alpha-loweralkylfurocoumarins and novel intermediates produced therein
abstract ABSTRACT OF THE DISCLOSURE .alpha.-Loweralkylfurocoumarins are produced by forming a .beta.-haloalk-2-enyl, e.g., .beta.-haloallyl, ether of a hydroxycoumarin having an active hydrogen in the position ortho to the hydroxy group, and heating the formed ether, preferably in dimethylaniline or like basic amine solvent. An abnormal Claisen rearrangement produces a novel o-hydroxy-(.beta.-haloalk-2-enyl)coumarin inter-mediate which can be dehydrohalogenated directly without isolation to the desired .alpha.-loweralkylfurocoumarin, e.g., .alpha.-methylfurocoumarin.
priorityDate 1979-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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