http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110627696-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-09
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C323-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-1804
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-1892
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C319-20
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C319-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-56
filingDate 2019-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110627696-B
titleOfInvention (Z) -4-difluoroalkyl-5-sulfanyl-4-pentenone derivative and preparation method thereof
abstract A (Z) -4-difluoroalkyl-5-sulfanyl-4-pentenone derivative is prepared from alkyne thioether with structure of formula (II), monobromodifluoroacetate, iridium face-tri (2-phenylpyridine), alkali and solvent through mixing, radiating by blue light to form reaction system, and post-treating to obtain the (Z) -4-difluoroalkyl-5-sulfanyl-4-pentenone derivative with structure of formula (I). The invention realizes the series reaction of addition-hydrogen migration-non-cyclization of free radicals to non-terminal alkyne for the first time and realizes the stereoselective synthesis of the (Z) -4-difluoroalkyl-5-sulfanyl-4-pentenone derivative in one step. The method has the advantages of mild reaction conditions, wide substrate application range, good reaction yield, simple operation and capability of synthesizing the fluorine-containing pentanesThe synthesis of the ketene compounds provides a new approach.
priorityDate 2019-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 59.