http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-256693-A1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-78
filingDate 1985-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8ca7eda236b0886d3138386736bf4226
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_77a3406790b6e0fcaf71e61ffcc33b09
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e5673665d83458cdeacea0bf21b5051
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1217ecf3a844f2f8ca3501bce1fdcd9f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb76ba00f5f4915dbb7b3bfa4549076d
publicationDate 1988-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DD-256693-A1
titleOfInvention PROCESS FOR PREPARING CYANIMIDODITHIOCHOKENOEENESTERS
abstract The invention relates to a process for the preparation of Cyanimidodithiokohlensaeureestern of the general formula III, in which R 1 is alkyl, alkenyl or aralkyl, R 2 aryl or hetaryl, which may optionally be substituted andX oxygen or sulfur. According to the invention, monoester potassium salts of the general formula I are first of all chloromethylated with a 20-30-fold molar excess of bromochloromethane in the presence of 0.5 to 2 mol% of a phase transfer catalyst such as triethylbenzylammonium bromide at temperatures between 30C and 60C, and the resulting chloromethyl cyanimidodithiocarbonate the general formula II then reacted with alkali metal thiolates or phenolates. Formulas (I), (II) and (III)
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5610311-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7157017-B2
priorityDate 1985-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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