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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D345-00
filingDate 2008-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2010-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e5289e1bf051e78a2802f78d38656eaa
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fbb229e84460f0145b3afb4dbc2f27e7
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publicationDate 2010-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2383538-C1
titleOfInvention METHOD FOR SYNTHESIS OF 1,2,3,4,5,6,10,11,12,13,14,15,15a,15b-TETRADECAHYDRODICYCLONONE [b, d] SELENOPHENE
abstract FIELD: chemistry. n SUBSTANCE: method for synthesis of 1,2,3,4,5,6,10,11,12,13,14,15,15a,15b-tetradecahydrodicyclonone[b,d]selenophene with general formula (1): n involves reacting cyclonone-1,2-diene with ethyl aluminium dichloride (EtAlCl 2 ) in the presence of Mg (powder) and a zirconocene dichloride catalyst (Cp2ZrCl 2 ), taken in molar ratio cyclonone-1,2-diene: EtAlCl 2 : Mg: Cp 2 ZrCl 2 -20:(11-13):20:(1.0-1.4), preferably 20:12:20:1.2. The reaction is carried out in an argon atmosphere at room temperature (20-22°C) and atmospheric pressure for 6-8 hours in tetrahydrofuran, with subsequent addition of an amount of selenium (Se) which is equimolar to EtAlCl 2 , benzene as a solvent and heating the reaction mass for 7 hours at temperature of approximately 80°C. n EFFECT: obtaining a compound with high selectivity. n 1 cl, 1 ex, 1 tbl
priorityDate 2008-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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