http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114085261-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_02ec105ea6a151157ba165830e5a8583
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J71-0031
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J71-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J7-00
filingDate 2021-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_196cdac361e127f394509d14d56bd5f0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11a97e305511839d30523511bbee3f83
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cfa9ab1ad3baec00f6bf30574e761ddb
publicationDate 2022-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-114085261-A
titleOfInvention A kind of preparation method of benzoprogesterone and intermediate thereof
abstract The invention belongs to the technical field of preparation of steroid hormone drugs, and in particular relates to a preparation method of benzoprogesterone, comprising using 4-AD as a starting material, and obtaining through acetylene reaction, catalytic hydration reaction, oxidation reaction and ketal reaction to obtain The target product, benzoprogesterone, wherein the catalytic hydration reaction is the catalytic hydration reaction of an acetylenic reactant and a copper salt under the catalysis of an acid, and the reaction is carried out at 25-55° C. for 3-5 hours to obtain a catalytic hydrate. Compared with the existing process route, the invention has the advantages of cheap and easy-to-obtain raw materials, and can avoid the use of highly toxic reagents such as osmium tetroxide, acetone cyanohydrin and the like.
priorityDate 2021-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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