CH279910A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH279910A CH279910A CH279910DA CH279910A CH 279910 A CH279910 A CH 279910A CH 279910D A CH279910D A CH 279910DA CH 279910 A CH279910 A CH 279910A
- Authority
- CH
- Switzerland
- Prior art keywords
- monoazo dye
- blue
- parts
- preparation
- dye
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Monoazofarbstoffes. Es wurde gefunden, dass man zu einem wertvollen Monoazofarbstoff gelangt, -wenn man diazotiertes 4-Nitro-6-aeetylamino-2- amiiio-l-ox#rbenzol in alkalischem Medium mit <B>1</B> -Plien#-Iaii-iino-8-o.xvnaphthalin-4 <B>-</B> sulfonsäure vereini( gt.
Der neue Farbstoff löst sieh in verdünnter Natriurnearbonatlösung mit blaugrauer, in konz. Schwefelsäure mit blauroter Farbe und färbt Wolle nach dem Nachehromierverfahren in licht- und waschechten grünen Tönen.
Die Diazotierun- des 4-Nitro-6-aeetylamino- 2-amino-1 -oxybenzols kann nach üblichen, an sich bekannten Methoden, z. B. mit Hilfe von 31ineralsäure, insbesondere Salzsäure lind Na- triumnitrit, durchgeführt werden.
Die Kupplung wird in alkalischem, bei spielsweise alkalicarbonat- oder alkali- livdroxydalkalisehem Medium vorgenommen. <I>Beispiel:</I> 21,1 Teile 4-Nitro-6-aeetylamino-2-amino-l- oxybenzol werden in<B>100</B> Teilen Wasser auf geschlämmt und naeh Zugabe von 20 Teilen 30 %iger Salzsäure und Eis bei <B>5</B> bis 100 mit <B>25</B>
Volumteilen 411-Natriuimnitritiösung in üb- lieller Weise diazotiert. Die Suspension der Diazoverbindung wird durch Zugabe von Na- triumearbonat neutralisiert und hierauf lil- triert. Der erhaltene Filterkuehen wird in eine durch Eiszugabe auf Ol> abgekühlten Lösung von<B>33</B> Teilen 1-Phenylamino-8-oxynaphthalin- 4-sulfonsäure in<B>150</B> Teilen Wasser,
14 Teilen <B>30</B> 1/oiger Natriumhydroxydlösung und 12 Tei len wasserfreiem, Natriumearbonat eingetra gen. Man rührt bei langsam ansteigender Tem peratur, bis die Kupplung beendet ist, scheidet den Farbstoff durch Zugabe von Natriumehlo- rid vollständig ab und filtriert. Der mit <B>5</B> "/oiger Natriumehloridlösung gewaschene Fil- terkuehen wird getrocknet.
Process for the preparation of a monoazo dye. It has been found that a valuable monoazo dye can be obtained if diazotized 4-nitro-6-aeetylamino-2-amiiio-1-ox # rbenzene in an alkaline medium with 1 -Plien # -Iaii -iino-8-o.xvnaphthalin-4 <B> - </B> sulfonic acid combined (gt.
The new dye dissolves in dilute sodium carbonate solution with blue-gray, in conc. Sulfuric acid with a blue-red color and dyes wool in lightfast and washfast green shades using the re-homing process.
The diazotization of the 4-nitro-6-aetylamino-2-amino-1-oxybenzene can be carried out by customary methods known per se, eg. B. with the help of 31ineral acid, especially hydrochloric acid and sodium nitrite.
The coupling is carried out in an alkaline medium, for example alkali carbonate or alkali metal hydroxide alkali. <I> Example: </I> 21.1 parts of 4-nitro-6-aeetylamino-2-amino-l-oxybenzene are suspended in <B> 100 </B> parts of water and, after adding 20 parts, 30% iger hydrochloric acid and ice at <B> 5 </B> to 100 with <B> 25 </B>
Parts by volume of 411 sodium nitrite solution are diazotized in the usual way. The suspension of the diazo compound is neutralized by adding sodium carbonate and then filtered. The filter cow is poured into a solution of <B> 33 </B> parts of 1-phenylamino-8-oxynaphthalene-4-sulfonic acid in <B> 150 </B> parts of water, cooled by adding ice to oil,
14 parts of 30% sodium hydroxide solution and 12 parts of anhydrous sodium carbonate are introduced. The mixture is stirred at a slowly increasing temperature until the coupling is complete, the dye is completely separated off by adding sodium chloride and filtered. The filter cow washed with <B> 5 </B>% sodium chloride solution is dried.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH279910T | 1948-09-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH279910A true CH279910A (en) | 1951-12-31 |
Family
ID=4482428
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH279910D CH279910A (en) | 1948-09-03 | 1948-09-03 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH279910A (en) |
-
1948
- 1948-09-03 CH CH279910D patent/CH279910A/en unknown
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