http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-938540-A1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_68dbe5a1efbe25eac632c950b785621c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0ec8f3b08e159c1a7c21b3fb2b49983c
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B1-16
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-53
filingDate 1980-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1983-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cdd0f5a996ec65add15d188755a4374c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7f5dba62887d2598ca6a2b00a23e4dd
publicationDate 1983-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-938540-A1
titleOfInvention Method forobtaining substituted 4,8-diamino-1,5-dioxiantraquinone
abstract METHOD OF OBTAINING SUBSTITUTED 4,8-DIAMINO-1,5-DIOXIANTHRAINAL Total volume number #% О О О О, IK: -; l R-hydrogen, alkyl, by sulphonating lu5-dioxyl 1,5-dimethoxyanthraquinone in oleum at 110-120s, followed by amination of the product in sulfuric acid in the presence of a vanadium catalyst and, if necessary, condensing the resulting 4,8-diamino-1 , 5-dioxy-; anthraquinone-2,6-disulfonic acid with compounds of the formula OOVOR, where R has the indicated values, fi sulfuric acid in the presence of boric acid, characterized in that, in order to intensify the hfotsess, amination is carried out in the presence of a cocatalyst selected from the group of transition metals: salts iron (li), iron (III), copper (II), in the amount of 10-60 mol.% of the amount of vanadium catalyst. U) eo; l li
priorityDate 1980-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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