http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S61155353-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C53-15
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-65
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filingDate 1984-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c950ce012ff8e9eb1fe0aded8e2c1a52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aab46e61d0b1d818ce81992146c5797a
publicationDate 1986-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S61155353-A
titleOfInvention Beta, beta-difluoro-gamma,delta-unsaturated carboxylic acid ester
abstract NEW MATERIAL:A compound shown by the formula I (R 1 WR 4 are H, alkyl, or R 1 and R 3 may be linked to form ring; R 5 is lower alkyl). n EXAMPLE: 3,3-Difluoro-4-hexadecenoic acid methyl ester. n USE: An intermediate for synthesizing especially a β,β-difluoro saturated carboxylic acid, a β-oxidation inhibitor to inhibit β-oxidatation in substance metabolism in a biochemical field. n PREPARATION: For example, an α-acetoxyaldehyde or ketone shown by the formula II is difluoromethylated with (Me 2 N) 3 P and CF 2 Br 2 in a solvent such as tetrahydrofuran, etc., to give a compound shown by the formula III, which is then saponified to give a 1,1-difluoro-1-alkene-3-ol shown by the formula IV. This compound is subjected to Claisen rearrangement in a solvent such as toluene, etc., in the presence of R 4 CH 2 C(OR 5 ) 3 and a propionic acid CH 3 CH 2 COOH acid to give a compound shown by the formula I. n COPYRIGHT: (C)1986,JPO&Japio
priorityDate 1984-12-27-04:00^^<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: 28.