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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J7-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J27-22
filingDate 1980-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d9e40ae2de6784c1ce22ee8fdcc4a72
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publicationDate 1982-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5798298-A
titleOfInvention Preparation of 17beta-ethinylsteroid
abstract PURPOSE: To prepare the titled compound useful as an intermediate for hydrocortisone, prednisolone, etc., economically in an industrial scale, by hydrolyzing 17α-ethinylsteroids using a cuprous salt in place of conventional expensive silver nitrate as a catalyst. n CONSTITUTION: A steroid having the partial structure of formulaI[X is -ONO 2 , -ONO, or OSO 2 R (R is alkyl or aryl)]e.g. 17α-ethinyl-17β-nitroxyandrosta-1, 4-dien-3-one, is hydrolyzed with water in the presence of a coprous salt (e.g. cuprous chloride) pref. at 30W80°C to obtain the objective compound having the partial structure of formula II (e.g. 17β-ethinyl-17α-hydroxyanodrosta-1,4-dien- 3-one). The amount of the cuprous salt is pref, 0.05W0.4 mole per 1 mole of the steroid used as the raw material. n EFFECT: The use of highly toxic sodium cyanide is not necessary. n COPYRIGHT: (C)1982,JPO&Japio
priorityDate 1980-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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