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filingDate 1976-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1978-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df0e61458ea3755d12ea28fa8b0e25bf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef4cbb1c8ab3e78ab5d7804206d4be4b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_464cba3127e6e698b7e8b26c15e452c4
publicationDate 1978-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4127728-A
titleOfInvention Preparation of 1-phenyl-2,2,2-trihalogeno-ethanol esters
abstract A process for the preparation of a substituted 1-phenyl-2,2,2-trihalo-ethanol ester of the formula <IMAGE> in which R is alkyl, halogenoalkyl, alkoxy, cycloalkyl or optionally substituted phenyl, benzyl, phenoxy, or phenylsulfonyl, X is halogenoalkyl with 1-3 carbon atoms and 1-3 halogen atoms, Y is halogen, cyano, nitro, alkyl, alkoxy, alkylmercapto, sulfoalkoxy or optionally substituted methylenedioxy, and N IS AN INTEGER FROM 0 TO 3, COMPRISING REACTING A COMPOUND OF THE FORMULA <IMAGE> WITH A HALOGENATED ALDEHYDE OF THE FORMULA X CHO in the presence of a Friedel-Crafts catalyst at a temperature of about -70 to +100 DEG C thereby to form a complex alcoholate, and reacting the complex alcoholate with an acid halide of the formula <IMAGE> OR WITH A CORRESPONDING ACID ANHYDRIDE AT A TEMPERATURE OF ABOUT -70 TO +100 DEG C. The reaction with the acid halide or anhydride is preferably carried out in the presence of a solvent or diluent, sodium sulfate hydrate is added to the final reaction solution and the resulting mixture of sodium sulfate and basic aluminum halide is filtered off. The products are known insecticides.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4277617-A
priorityDate 1975-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 383.