http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2646884-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C307-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C307-02
filingDate 1976-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2469f23a22fd494cd275707fd15a4978
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc00c6a5110832e0345d1bfdfa0e6c16
publicationDate 1978-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2646884-A1
titleOfInvention PROCESS FOR PRODUCING SULFUR ACID DIAMIDES
abstract Sulphuric acid diamides of formula R-C6H4-NH-SO2-NME (I) (where R is H, Me, F or Cl) are prepd. by reacting dimethylamino-sulphochloride having formula Cl-SO2-NMe2 (II) with an aniline having formula R-C6H4-NH2 (III), in the presence of inorganic reducing agents, (IV), and of acid binders, at pH 3-5, 40-80 (45-70) degrees C, in water as diluent. (I) are intermediates in synthesis of pesticides, plant-protective fungicides and dyes. (i) Addn. of (IV) gives a smooth, quicker reaction. (ii) Highly pure (I) is obtd., requiring no further purificn., the moisture content being low. (ii) Cooling may take place by using warm industrial recycle water. In an example, use of NaHSO3 as (IV), in prepn. of PhNH-SO2-NME2 from (II) and aniline, increases yield from 82- to 92%; reduces reaction time from 30- to 20 hrs., increases purity to 99% and reduces moisture content from 25- to 8%.
priorityDate 1976-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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