http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2433990-C2

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C35-21
filingDate 2009-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1cc6c33fd4556a6d82503df417ff458d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_912accf1d62ea5ffa9defd73e9b7aeb4
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publicationDate 2011-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2433990-C2
titleOfInvention Method of producing 1-alkyl-2-alkyl(cycloalkenyl, benzyl)cyclopropanols
abstract FIELD: chemistry. n SUBSTANCE: invention relates to a method of producing 1-alkyl-2-alkyl(cycloalkenyl, benzyl)cyclopropanols of general formula (I): n R=C 6 H 13 , R'=CH 3 , C 2 H 5 , C 4 H 9 , n , ; n which can be used in fine organic synthesis, particularly synthesis of biologically active compounds, having pyrethroid, acaricide, pesticide, growth-regulating, fungicide and anti-bacterial activity. The method involves catalytic reaction of olefin with an organometallic compound and an ester. The organometallic compound used is ethylaluminium dichloride (EtAlCl 2 ). Reaction of α-olefin of general formula R-CH=CH 2 , where R=C 6 H 13 , , n with an ester of formula R'CO 2 R", where R'=CH 3 , C 2 H 5 , C 4 H 9 ; R"=Me, Et and EtAlCl 2 is carried out in the presence of Mg (powder) and a Cp 2 ZrCl 2 catalyst in molar ratio R-CH=CH 2 : R'CO 2 R":EtAlCl 2 :Mg:Cp 2 ZrCl 2 =10:10:(20-30):(10-14):(0.8-1.2) in an argon atmosphere at temperature 20-22°C and atmospheric pressure for 8-12 hours. n EFFECT: method enables to obtain desired products with high regioselectivity. n 1 tbl, 14 ex
priorityDate 2009-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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