http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4416834-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-1651
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-165
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N57-12
filingDate 1980-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1983-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2e05d7e4e6a3ceecb693f4a45eb4502c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2e61e882336413c770b15057b19a7f0b
publicationDate 1983-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4416834-A
titleOfInvention Process for the preparation of thiophosphoric acid esters
abstract A process for the preparation of a compound of the formula ##STR1## in which R is alkyl, n X is oxygen or sulphur and n R' is hydrogen or alkyl, n comprising reacting a thiophosphate of the formula ##STR2## in which M is a cation other than NH 4 .sup.⊕, with an ethylmercapto compound of the formula ##STR3## in which Y is a fugitive group, in a polar reaction medium at a temperature between about 30° and 80° C. and at a pH between about 2 and 9. Advantageously X is oxygen and the thiophosphate is produced by reaction of a dialkyl phosphite of the formula ##STR4## with sulphur in the presence of an organic base in an organic solvent and subsequent extraction with aqueous MOH solution. Also Y is advantageously chlorine and the ethylmercapto compound is prepared by heating the corresponding alcohol to about 40°-100° C. and passing hydrogen chloride gas into the pre-warmed alcohol, the reaction solution being used directly without working up.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004176629-A1
priorityDate 1979-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID69820
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID977
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226453373
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393705
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID480707
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID1008838
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448072971
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226397689
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID61797
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6893
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID390985
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID96861
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID13068
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226406159
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523291
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID7111

Total number of triples: 309.