http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2747675-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-03
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-03
filingDate 1996-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_83bf445004e3304674ed08de066ccda0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b4332aad0e0c6f0c7ce5d69bb372fbca
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd07b60179a2c70e0e68b4f9614899a7
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publicationDate 1997-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FR-2747675-A1
titleOfInvention PROCESS FOR THE PREPARATION OF (METH) ACRYLATES
abstract A compound (I) is prepared by reacting a compound (II) with an alcohol (III) in the presence of a catalytic system comprising: as catalyst, at least one zirconium compound chosen from zirconium alcoholates Zr (OR * * 7) 4 (R ** 7 = C1 -C6 alkyl); ZrO2; ZroC12; and ZrX4 (X = halogen); and at least one dopant chosen from beta-diketones; beta-ketonic acid esters; and beta-hydroxyketones; the dopant (s) which can be introduced initially or during the reaction. (CF DRAWING IN BOPI) R ** 1 = H or methyl; R ** 2 = C2-C30 alkyl; (C1-C30 alkoxy) C1-C30 alkyl; allyl; -R ** 3-NR ** 4R ** 5 (R ** 3 = C2 -C4 hydrocarbon chain; R ** 4, R ** 5 = alkyl or aryl); (CF DRAWING IN BOPI) (A, B = C2-5 alkylene; benzyl; R ** 6 = C1 -C10 alkyl, lower than the alkyl group entering into the definition of R ** 2 when a transesterification is carried out aiming to obtain a compound (I) for which R ** 2 = C2 -C30 alkyl.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-03022796-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6288255-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-19940622-C1
priorityDate 1996-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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