http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2938457-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C49-813
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-46
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-813
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filingDate 1979-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_704871160390efb10767f6b62d763ff3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a01187adcbdc32dca973fb37ec40d8f8
publicationDate 1981-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2938457-A1
titleOfInvention METHOD FOR PRODUCING A HALOGENATED BENZOPHENONE, THE PRODUCT OBTAINED THEREOF AND THE USE THEREOF
abstract In a new process for the prodn. of a 2-(chloro- or bromo)-4'- (fluoro-, chloro- or bromo)-benzophenone (I), fluoro- chloro- or bromo-benzene (II) is reacted with an approximately equimolar amt. of a 2-(chloro- or bromo) benzoyl halide (III) in the presence of an aluminium halide, then the reaction prod. is hydrolysed and resulting (I) is isolated in the usual manner and opt. purified (where X is F, Cl or Br; and Y is Cl or Br). (I) are useful as intermediates for pharmaceuticals and plant protection agents, esp. fungicidal triphenylmethane derivs. The process can be carried out in the absence of solvents or diluents, thus avoiding the risk of fire or explosion. Yields are good, and (I) are obtd. in good purity.
priorityDate 1979-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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