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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-80
filingDate 1998-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_01301fc7a51659328361583d2ee389b8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42fb9506781a022956d6e2ad2aa07621
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e6476aa5f0680b4f53184cebc3c8c251
publicationDate 2001-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6184417-B1
titleOfInvention Method for preparing acetophenones with a fluoralkyl-substituted aromatic nucleus
abstract Acetophenones which are substituted on the aromatic ring by fluoroalkyl are prepared in a particularly advantageous, environmentally friendly and effective manner from fluoroalkylanilines and acetaldoxime by preparing from a fluoroalkylaniline a corresponding diazonium salt solution, and reacting this with acetaldoxime in the presence of at least one copper compound, without adding any buffer salts or reducing agents, carrying out the reaction at from 20 to 50° C. and in the presence of halide ions and subsequently heating to a temperature in the range from 70 to 110° C.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6670496-B1
priorityDate 1997-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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