http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0143613-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5ac17835c97e6c72213815ca74845386
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C263-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C265-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C263-10
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C265-06
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C263-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C265-04
filingDate 1984-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_85b2ca359e6b174a7d5a9359092e0bc2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fafa22200c058ca9025cf492b5073a00
publicationDate 1985-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0143613-A2
titleOfInvention Production of isocyanate compounds
abstract Production of an alkenoyl isocyanate of the formula:wherein R is a hydrogen atom or a lower alkyl group by reacting an acrylamide of the formula:wherein R is as defined above with an oxalyl halide of the formula:wherein X is a halogen atom to give a reaction mixture comprising a haloalkanoyl isocyanate of the formula:wherein R and X are each as defined above with or without the alkenoyl isocyanate, recovering the haloalkanoyl isocyanate and, when present, the alkenoyl isocyanate separately from the reaction mixture and reacting the recovered haloalkanoyl isocyanate with a hydrogen halide-eliminating agentto give the alkenoyl isocyanate.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5496943-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0617025-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0671385-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0503958-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0202840-A2
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priorityDate 1983-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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