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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5c24684033fba97d1ad845ce453a57e3
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-34
filingDate 1984-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1987-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b4a76cc845acf4c446a7c0ee7cc4ad9e
publicationDate 1987-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1230885-A
titleOfInvention Process for preparing organic chlorophosphanes
abstract Abstract or the Disclosure Organic chlorophosphanes of the formula III (III), in which R1 is chlorine or an aliphatic radical, prefer-ably only chlorine, and R2 is an aromatic, heterocyclic or aliphatic radical, are prepared by reacting organic phosphorus oxychlorides of the formula I in which R1 is chlorine or an aliphatic radicai, prefer-ably only chlorine, R2 is an aromatic or heterocyclic radical in the event that R1 is chlorine and an aromatic, heterocyclic or aliphatic radical in the event that R1 is an aliphatic radical, with a trialkylphosphane of the formula II (II) in which R3 is an aliphatic rac1ical, at temperatures between about 20 and about 170°C. said organic chlorophosphanes III are mai1nly intermediates in various fields, such as pharmaceuticals, plant protection, dyestuffs and polymers.
priorityDate 1983-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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