http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0436183-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b94baf1aad802afc19b0e63b4499b04d
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C255-65
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-65
filingDate 1990-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f0e98a952279ca3bb16d764bd1dd8f2b
publicationDate 1991-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0436183-A1
titleOfInvention Process for the preparation of symmetrical azodinitrile dicarboxylic acids from keto acids
abstract The preparation of symmetrical azodinitriles prepared from keto acids is disclosed. A keto acid of the formulan n is reacted with M(CN) x and an ammonia source to obtain an aminonitrile metal carboxylate of the formulan n The aminonitrile metal carboxylate is reacted with M₁(OCl) x with the proviso that no alcohol or surface active agent is utilized to form a metal salt of an azo compound. This metal salt is reacted with mineral acid to give the symmetrical azodinitrile compound of the formulan n R₁ is an alkyl group containing from 1 to about 12 carbon atoms and R₂ is an alkylene group containing from 1 to about 12 carbon atoms. M is a metal comprising lithium, sodium, potassium, magnesium or calcium; M₁ is a metal comprising sodium, potassium or calcium; and x is the valence of M and M₁. In other embodiments, the preparation of mixed, symmetrical azonitrile initiators and mixed azodinitrile initiators via hydrazo intermediates, prepared from keto acids and aminonitrile and keto acids and a hydrazine source, a ketone and hydrochloric acid respectively is disclosed.
priorityDate 1989-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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