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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C55-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-567
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-63
filingDate 1994-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2aefe86a100ad56c1f37168083431fe1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_08a4aaf231c52134b62cf40858bd2793
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_babc1fe6ab4221dfccabdb5f97cae252
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publicationDate 1995-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H07285916-A
titleOfInvention Method for producing α, α′-dichloroadipic acid diester
abstract (57) [Summary] (Modified) [Structure] Polyadipic acid polyanhydride is reacted with chlorine in the presence of a solvent to produce α, α'-dichloropolyadipic acid polyanhydride, which is then obtained. Α, α ′ of the formula (IV) characterized by reacting an anhydride with an alcohol in the presence of a solvent, and performing a series of steps in one pot -Method for producing dichloroadipic acid diester. (In the formula, R represents a linear or branched alkyl alcohol having 1 to 12 carbon atoms, an aryl alcohol, or an aralkyl alcohol.) [Effect] Using this production method, polyadipic acid polyanhydride and chlorine are used in a solvent. By reacting with and, by-products are significantly reduced, and as a result, α, α′-dichloroadipic acid polyanhydride can be obtained with high selectivity and in good yield. Furthermore, by continuously reacting with alcohol in a solvent and esterifying, α, α′-dichloroadipic acid diester can be obtained with a high selectivity and a high yield, and can be obtained in one pot, which has an extremely high industrial value. large.
priorityDate 1994-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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