JPH0119425B

1. Process for the preparation of copper complex azo dyestuffs from azo dyestuffs of the formula see diagramm : EP0063739,P5,F2 wherein A = an optionally further substituted phenyl or naphthyl radical having an unsubstituted o-position relative to the azo group, and B = the radical of a coupling com...

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Hauptverfasser: RAINAA DEITSUTSUAA, HERUMAN HENKU, BORUFU ETSUKUHARUTO BURETSUKU, KARURU HAINTSU SHUNDEHYUTSUTE
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creator RAINAA DEITSUTSUAA
HERUMAN HENKU
BORUFU ETSUKUHARUTO BURETSUKU
KARURU HAINTSU SHUNDEHYUTSUTE
description 1. Process for the preparation of copper complex azo dyestuffs from azo dyestuffs of the formula see diagramm : EP0063739,P5,F2 wherein A = an optionally further substituted phenyl or naphthyl radical having an unsubstituted o-position relative to the azo group, and B = the radical of a coupling component having a phenolic or enolic OH group in the o-position relative to the azo group, in particular the radical of a coupling component of the phenol, naphthol, pyrazole, pyrazolone, pyridone or aceto-acetic acid arylide series, characterised in that oxidative coppering is carried out in a weakly acid medium in the presence of lithium carbonate.
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Process for the preparation of copper complex azo dyestuffs from azo dyestuffs of the formula see diagramm : EP0063739,P5,F2 wherein A = an optionally further substituted phenyl or naphthyl radical having an unsubstituted o-position relative to the azo group, and B = the radical of a coupling component having a phenolic or enolic OH group in the o-position relative to the azo group, in particular the radical of a coupling component of the phenol, naphthol, pyrazole, pyrazolone, pyridone or aceto-acetic acid arylide series, characterised in that oxidative coppering is carried out in a weakly acid medium in the presence of lithium carbonate.</description><language>eng</language><subject>ADHESIVES ; CHEMISTRY ; DYES ; LAKES ; METALLURGY ; MISCELLANEOUS APPLICATIONS OF MATERIALS ; MISCELLANEOUS COMPOSITIONS ; MORDANTS ; NATURAL RESINS ; ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES ; PAINTS ; POLISHES</subject><creationdate>1989</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19890411&amp;DB=EPODOC&amp;CC=JP&amp;NR=H0119425B2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19890411&amp;DB=EPODOC&amp;CC=JP&amp;NR=H0119425B2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>RAINAA DEITSUTSUAA</creatorcontrib><creatorcontrib>HERUMAN HENKU</creatorcontrib><creatorcontrib>BORUFU ETSUKUHARUTO BURETSUKU</creatorcontrib><creatorcontrib>KARURU HAINTSU SHUNDEHYUTSUTE</creatorcontrib><title>JPH0119425B</title><description>1. 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Process for the preparation of copper complex azo dyestuffs from azo dyestuffs of the formula see diagramm : EP0063739,P5,F2 wherein A = an optionally further substituted phenyl or naphthyl radical having an unsubstituted o-position relative to the azo group, and B = the radical of a coupling component having a phenolic or enolic OH group in the o-position relative to the azo group, in particular the radical of a coupling component of the phenol, naphthol, pyrazole, pyrazolone, pyridone or aceto-acetic acid arylide series, characterised in that oxidative coppering is carried out in a weakly acid medium in the presence of lithium carbonate.</abstract><oa>free_for_read</oa></addata></record>
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subjects ADHESIVES
CHEMISTRY
DYES
LAKES
METALLURGY
MISCELLANEOUS APPLICATIONS OF MATERIALS
MISCELLANEOUS COMPOSITIONS
MORDANTS
NATURAL RESINS
ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES
PAINTS
POLISHES
title JPH0119425B
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