http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-19612188-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7ae1f43fedfc45bc134632d798f08b85 |
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 |
Incoming Links
Total number of triples: 73.