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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-1406
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C309-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-14
filingDate 1969-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e125a82ca80ba7c3507c6e8d5cd13c39
publicationDate 1971-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-1943534-A1
titleOfInvention Process for the preparation of hydroxynaphthalenesulfonic acids
abstract Hydroxynaphthalene sulphonic acids used in axo-dyestuffs manufacture. (A) R' = POCl2, R2 = R3 =H, (B) R' = POCl2, R2 = SO3H, R3 = H, (C) R' = POCl2, R2 = R3 = SO3H, (D) R' = R3 = H, R2 = SO3H, (E) R' = H, R2 = R3 = SO3H. alpha- and beta-naphthol give (IA) and (IIA) respectively with POCl3. Sulphonation, pref. with H2SO4, ClSO3H or oleum at 0-130 degrees C, then gives (IB) and (IIB) respectively; or (IC) and (IIC) respectively if >2 moles, pref. 3.5 moles, of sulphonating agent are used. Hydrolysis yields (ID), (IE), (IID) and (IIE) respectively. These compounds are useful as coupling components for azo-dyestuffs. No by-products formed as in previous syntheses.
priorityDate 1969-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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