http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002156290-A1

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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>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a01c3d6a6f6220dc8fa8a6779b0110b5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1381431e5ad113f60d8397139b5cddee
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f3ce5d64c52ccfa12aabc8f31b0a43ef
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_61a6b9ce9e9ef71716743f6c814c023c
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_61e1ee0c34684452e0b0b6807789d5d3
publicationDate 2002-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2002156290-A1
titleOfInvention Preparation of 2-alkyl-3-(4,5-dihydroisoxazol-3-yl) halobenzenes
abstract A novel process for preparing the compounds of the formula I n n n where: n n is 0, 1 or 2; n R 1 ,R 2 are C 1 -C 6 -alkyl; n R 3 ,R 4 ,R 5 are hydrogen or C 1 -C 6 -alkyl, or R 4 and R 5 together form a bond; n R 6 is Cl, Br, n which comprises a synthesis sequence starting from 1,2-dialkylbenzenes of the formula II n n n with subsequent halogenation to give 3,6-dihalo-1,2-dialkylbenzenes, haloalkylation to give benzyl bromides, oxidation to give benzaldehydes, oximation, reaction 40 with alkenes to give isoxazoles, conversion into thioethers and, if appropriate, oxidation to give sulfenyl or sulfonyl derivatives of the formula I.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114057715-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112125898-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110642689-A
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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