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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C253-30
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-30
filingDate 1996-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c9f844458c41348a8f2ad76eeb63894
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ac637ebdd8da7032e1745b4af062b3b9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d346d98de1951e8b1e379dea1e911998
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb5d452a5a144e3e5573892602e2da5e
publicationDate 1996-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-19612188-A1
titleOfInvention Process for the preparation of 2-cyanoacrylic acid
abstract Prodn. of 2-cyanoacrylic acid (I) comprises the trans-esterification of a 2-cyanoacrylate (II) with an organic acid. Pref. the trans-esterification of (II), esp. the methyl, ethyl, n-propyl, isopropyl, n-butyl and/or isobutyl ester, is conveniently carried out using formic, acetic, propionic and/or butyric acid, esp. acetic acid, as the organic acid. It is conveniently carried out in the presence of a cation exchange resin as a catalyst, suitably at 10-130 deg C, esp. 40-90 deg C. The molar ratio of organic acid to (II) is typically 50:2, and 20-70 wt.% catalyst is advantageously used based on the total wt. of the reaction mixt..
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-102009000861-A1
priorityDate 1995-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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