http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0434175-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_396f4d1c26d73c650d53c4d5fc00c46b
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-08
filingDate 1990-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_636fda1574e625c0c8859df9d2a02ef9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad7117c4ec7bf4f761888165083b5465
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6756b0d754ef3970382a1b5ea2df6ae8
publicationDate 1991-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0434175-A1
titleOfInvention Sulphobetain-substituted alpha-sulphonyl carboxylic acids from diallylammonium salts and process for their preparation
abstract The invention relates to new sulfobetaine-substituted α-sulfonylcarboxylic acids of the general formula I and processes for their preparation. As organic intermediates, the compounds of formula I represent a reactive synthesis building block with sulfobetaine character and can be used for further syntheses. In the case of long-chain alkyl radical R 1, polyfunctional surfactants are obtained. According to the invention, molar amounts of diallylammonium chloride are reacted with chloroacetic acid and the double-molar amount of sodium hydrogen sulfite in the presence of a catalytic amount of a peroxodisulfate, and the reaction solution obtained, after addition of a catalytic amount of iodide, is converted by heating to sulfobetaine-substituted α-sulfonylacetic acids according to general formula I.
priorityDate 1989-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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