http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111187154-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C253-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C63-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-38
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-57
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C57-58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C63-68
filingDate 2019-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-111187154-B
titleOfInvention Synthetic method of sitagliptin intermediate 2,4, 5-trifluoro phenylacetic acid
abstract The invention provides a synthetic method of a sitagliptin intermediate 2,4, 5-trifluoro phenylacetic acid, which comprises the steps of substitution reaction, hydrolysis reaction and decarboxylation reaction, wherein A, a compound of a formula 5 is prepared by the substitution reaction of a compound 4, or the substitution reaction and the hydrolysis reaction of the compound; B. carrying out hydrolysis reaction on the compound shown in the formula 5 to prepare a compound shown in a formula 6; C. the 2,4, 5-trifluoro-phenylacetic acid is prepared by decarboxylation reaction of a compound shown in a formula 6 under the catalysis of a catalyst, wherein the catalyst is a metal oxide. The synthesis process has low cost, high yield and strong applicability in industrial scale-up production, and can be used for preparing the 2,4, 5-trifluoro-phenylacetic acid compound.
priorityDate 2018-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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