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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D261-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-04
filingDate 1999-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6edb93a2acf9ee6a9d817b681bee4807
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_53cc5a261c4d9098beb12c107c960623
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d471cd0644a18551fa19206819295173
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_24e8d6f922437f0f78c8e00afdbda66a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_893c74de2a42dbcb2401f344a42ead4d
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4c06cc586ec900b0f027af0611c002e3
publicationDate 2000-05-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2351466-A1
titleOfInvention Method of producing 2-alkyl-3-(4,5-dihydroisoxazole-3-yl)-halobenzenes
abstract The invention relates to a novel method of producing the compounds of formul a (I) wherein the substituents have the following meanings: n is 0,1 or 2; R1, R2 represent C1-C6-alkyl; R3, R4, R5 are hydrogen, C1-C6-alkyl or R4 and R5 together form a bond; R6 is C1, Br. Said method comprises the following step s: a synthesis sequence starting from 1,2-dialkylbenzenes of formula (II); halogenation to form 3,6-dihalogen-1,2-dialkylbenzenes; haloalkylation to fo rm benzyl bromides; oxidation to form benzaldehydes; reaction with alkenes to form isoxazoles; reaction to form thioethers and optionally oxidation to for m sulfenyl or sulfonyl derivatives of 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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