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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-301
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-30
filingDate 1977-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1978-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2affd51a6f34b282fb374c5a55f467d2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6be3123bdeebbcc10bf02af25437dfcf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e9181146d45f677657302328367d732c
publicationDate 1978-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4105689-A
titleOfInvention Production of N-substituted 2-carbamoyl phosphinic acids
abstract Production of N-substituted 2-carbamoyl phosphinic acids of the general formula: <IMAGE> (I) in which R1 stands for an alkyl group having 1 to 4 carbon atoms or an aryl group; R2 and R3 stand independently of each other for an alkyl group having 1 to 4 carbon atoms, an aryl group or a hydrogen atom; R4 stands for an alkyl group having 1 to 18 carbon atoms, an aryl group or a hydrogen atom; and R5 stands for an alkyl group having 1 to 18 carbon atoms or an aryl group. More specifically, a 2-chloroformyl phosphinic acid chloride of the general formula <IMAGE> (II) is reacted at 120 DEG to 170 DEG C with an amine of the general formula <IMAGE> (III) and resulting N-substituted 2-carbamoyl phosphinic acid chloride of the general formula <IMAGE> (IV) the latter compound being obtained while hydrogen chloride is split off, is hydrolyzed with water.
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priorityDate 1976-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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