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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-04
filingDate 2002-05-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2003-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d471cd0644a18551fa19206819295173
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f31a8e1661d3a89e6c7923aed56b50f4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f4ea6396cf5e5407de0c956c203ab22c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_24e8d6f922437f0f78c8e00afdbda66a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6edb93a2acf9ee6a9d817b681bee4807
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_893c74de2a42dbcb2401f344a42ead4d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4c06cc586ec900b0f027af0611c002e3
publicationDate 2003-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6603017-B2
titleOfInvention Preparation of 2-alkyl-3-(4,5-dihydroisoxazol-3-yl) halobenzenes
abstract A novel process for preparing the compounds of the formula Iwhere:n is 0, 1 or 2;R1, R2 are C1-C6-alkyl;R3, R4, R5 are hydrogen or C1-C6-alkyl, or R4 and R5 together form a bond;R6 is Cl, Br,which comprises a synthesis sequence starting from 1,2-dialkylbenzenes of the formula IIwith subsequent halogenation to give 3,6-dihalo-1,2-dialkylbenzenes, haloalkylation to give benzyl bromides, oxidation to give benzaldehydes, oximation, reaction with alkenes to give isoxazoles, conversion into thioethers and, if appropriate, oxidation to give sulfenyl or sulfonyl derivatives of the formula I.
priorityDate 1998-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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