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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C315-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C315-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C317-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
filingDate 1990-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1990-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b06ff9947399641b780139d4c18af221
publicationDate 1990-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4948917-A
titleOfInvention Process for the preparation of beta-chloroethylsulfonylaryl isocyanates
abstract Process for the preparation of β-chloroethylsulfonylaryl isocyanates of the formula (1) n n Cl--H.sub.2 C--H.sub.2 C--O.sub.2 S--A--NCO (1) n n wherein A is a phenylene radical, which can contain substituents from the series comprising alkyl(C 1 -C 6 ), alkoxy(C 1 -C 6 ), chlorine, bromine and nitro, or a naphthylene radical, by allowing at least 2 moles of phosgene to act on 1 mole of β-hydroxyethylsulfonyl-arylamine of the formula (2) n n HO--H.sub.2 C--H.sub.2 C--O.sub.2 S--A--NH.sub.2 (2) n n wherein A has the abovementioned meaning, in the presence of a catalyst at temperatures of about 100° to 200° C., if appropriate in an inert solvent.
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priorityDate 1989-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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