http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006508024-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-22
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-65
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-58
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filingDate 2003-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2006-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2006508024-A
titleOfInvention Improved process for the preparation of 2,2-dichloro- or dibromophenylacetic acid alkyl esters
abstract In an improved method for producing 2,2-dichloro- or -dibromophenylacetic acid alkyl ester represented by the formula (I) described in the specification, the compound represented by the formula (II) described in the specification is used. 2,2-dichloro- or -dibromophenylacetonitrile prepared with 0.8 to 2 mol of water per mol of nitrile of formula (II), 1 to 8 mol of R1OH (III) per mol of nitrile of formula (II) Reaction in the alcohol represented in the presence of 1 to 3 mol of HCl or HBr per mol of nitrile of the formula (II), optionally in the presence of a solvent which is inert under the reaction conditions, The corresponding 2,2-dichloro- or -dibromophenylacetic acid alkyl ester of the formula (I) is obtained, in which the reaction temperature in the first stage of the reaction is 30-60 ° C. and in the second stage 60-100 ° C. Characterized in that, after completion of the conversion, the reaction mixture is cooled to 20-40 ° C., diluted with water and the corresponding 2,2-dichloro- or dibromophenylacetic acid alkyl ester of the formula (I) is isolated The above method.
priorityDate 2002-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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