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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-72
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-65
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-84
filingDate 2012-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_839d5bef9dbd58653ec6e35fc3ad0b0e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_420057e15164d566e78186c3e187abf6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b996d9bf9feaaa312d5ca3fb08b70317
publicationDate 2013-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2475473-C1
titleOfInvention 3-phenoxyphenyl-containing 1,3-diketones as starting compounds for producing chelate complexes thereof with copper (ii) ions and method of producing 3-phenoxyphenyl-containing 1,3-diketones
abstract FIELD: chemistry. n SUBSTANCE: invention relates to the chemistry of diphenyl oxide derivatives and specifically to novel 3-phenoxyphenyl-containing 1,3-diketones, intermediate compounds in synthesis of a wide range of biologically active substances of general formula , for example as starting compounds for producing chelate complexes thereof with copper (II) ions of general formula , which have potential for use as extraction agents, analytical reagents of rare-earth elements, vital semiproducts in synthesis of probable biologically active substances. The invention also relates to a method of producing 3-phenoxyphenyl-containing 1,3-diketones, involving reaction of 3-phenoxybenzonitrile with lower alcohols: methanol, ethanol in molar ratio 1:4.245, respectively, in the presence of concentrated sulphuric acid for 7-8 hours, to form alkyl-3-phenoxybenzoate, and subsequent reaction thereof with ketones selected from: acetone, 2-butanone, acetophenone in molar ratio 2.0:1, respectively, in a medium of pure cyclohexane at boiling point thereof in the presence of catalytic amounts of sodium hydride for 2.5-3 hours, followed by extraction of the end product. n EFFECT: wider range of diphenyl oxide derivatives and obtaining 3-phenoxyphenyl-containing 1,3-diketones and chelate complexes thereof with copper (II) ions with high output. n 2 cl, 6 ex
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2529029-C1
priorityDate 2012-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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