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filingDate 1967-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a50cbe2c68839d6d45373342ff63d881
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ead492e1cb884593d402f4c120f0f010
publicationDate 1969-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1170514-A
titleOfInvention Cross-Linkable Copolymer Dispersions
abstract 1,170,514. Esters and amides containing chloromethyl and acrylic or methacrylic residues. FARBENFABRIKEN BAYER A.G. 31 Jan., 1967 [25 March, 1966], No. 4636/67. Heading C2C. [Also in Division C3] (a) Compounds of the formula CH 2 = CR-CO-NH-CH 2 -NHCO-CH 2 Cl (where R is H or methyl) are prepared by reacting equimolar amounts of N-methylolchloroacetamide and (meth)acrylamide in glacial acetic acid in the presence of cone. HCl and phenothiazine. (b) The compound of formula CH 2 = C(CH 3 ) -COO-CH 2 -CH(CH 3 )-OOC-CH 2 Cl is prepared by reacting equimolar amounts of #- hydroxypropyl methacrylate and chloroacetic acid in toluene in the presence of p-toluene sulphonic acid and 2,6-di-t-butylphenol-4-methylol methyl ether, while removing water of reaction azeotropically. (c) The compounds of formula CH 2 = C(CH 3 )- CO-A-CO-NH-CO-CH 2 Cl (where A is -NH- or -O-CH 2 -CH(CH 3 )-O-) are prepared by reacting equimolar amounts of chloromethylacylisocyanate and methacrylamide or #-hydroxypropyl methacrylate respectively in dry toluene.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4840991-A
priorityDate 1966-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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