http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CZ-20013406-A3

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_01fdc14f88476b2516248451fd695f1d
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-71
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-71
filingDate 2000-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aae02464dd799e82418f4169ae069026
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2988575f7e66121221d4d5b86ca2c66e
publicationDate 2002-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-20013406-A3
titleOfInvention Process for producing chlorides of chlorinated pyridine sulfonic acids
abstract The invention relates to a method of producing chloropyridine sulfonic acid chlorides of general formula (I) from hydroxypyridine sulfonic acids of general formula (II) by substituting the OH groups at the ring and the OH group of the acid group with a chlorinating agent. A mixture of phosphorus trichloride in an excess to a stoichiometric quantity and chlorine in a stoichiometric quantity to slightly less in relation to the hydroxypyridine sulfonic acid is used as the chlorinating agent. The chlorine is added to a mixture of hydroxypyridine sulfonic acid and phosphorus trichloride at temperatures of 70 to 90 DEG C. The mixture is heated to temperatures of 100 to 120 DEG C, the resulting phosphorus chloride oxide and optionally excess phosphorus trichloride are distilled off, the residue is dissolved in an organic solvent and the liquid phase is distilled under reduced pressure to obtain the chloropyridine sulfonic acid chloride.
priorityDate 1999-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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