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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C271-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C269-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C291-00
filingDate 1988-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_80197a9f1cc20ab52c6ed0472dfe9c99
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b1b60e1db6caa6c18e6cfea780fed5ba
publicationDate 1988-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0294686-A2
titleOfInvention Process for the preparation of diaryliminocarbonates
abstract Process for the preparation of iminocarbonic acid diaryl esters of the general formula I in the R¹ represents an alkyl, aminoalkyl, cycloalkyl, aralkyl, aryl group or a heterocyclic or heteroaromatic radical, Y and Z are the same or different and represent an alkyl, alkoxy, haloalkyl, aryl, cyano, nitro group or halogen, m and n represent an integer from 1 to 5, where, if m and n are greater than 1, the radicals Y and Z are the same or different, characterized in that diphenyl iminocarbonate II with a substituted phenol III at temperatures of 50 to 250 ° C to iminocarbonic acid diaryl esters IV and reacting the compounds IV after their isolation or in situ with a phenol substituted by Z or Y to give the end products I and new imino carbonic acid diaryl esters I and II and preparation of the diphenyl imino carbonic acid II by reacting dichlorodiphenoxime methane with a primary amine R 1 NH 2 in an inert solvent in the presence a base and optionally in the presence of a catalytic amount of N, N-dialkylaminopyridine.
priorityDate 1987-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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