CH169692A - Process for the preparation of an acid dye. - Google Patents
Process for the preparation of an acid dye.Info
- Publication number
- CH169692A CH169692A CH169692DA CH169692A CH 169692 A CH169692 A CH 169692A CH 169692D A CH169692D A CH 169692DA CH 169692 A CH169692 A CH 169692A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- amino
- acid dye
- acid
- Prior art date
Links
Description
verfahre. zur Herstellung eines Säurefarbstoffes. <B>Es</B> wurde gefunden, dass man neue, wert volle Farbstoffe vom Charakter der Säure farbstoffe erhält, indem man Azofarbstoffe, die durch alkalisches Kuppeln von 3-Amino- 1-oxybenzolen, deren 4-Stellung zur Hydro- xylgruppe unbesetzt ist;
mit wenigstens eine löslichmachende Sulfon- oder Carbonsäure- gruppe enthaltenden Diazoverbindungen erhal ten werden undkeinezurMetallkomplexbildung befähigte Gruppe enthalten, in alkalischer Lesung mit Oxydationsmitteln, vorzugsweise Kupferverbindungen, behandelt. Hierdurch er fahren dicAzofarbstoffeeineÄnderungin ihrem Ton und eine Verbesserung der Lichtecht heit der mit ihnen erzielten Färbungen.
Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Herstellung eines solchen Säurefarbstoffes, welches dadurch gekenn zeichnet ist, dass man den aus dianotierter 4 - Nitro - 4'- amino-diphenylamirr2-sulfosäure und 3-Amino-l-oxybenzol in sodaalkaliseher Lösung erhaltenen Farbstoff in alkalischer Lösung mit einem Oxydationsmittel behan delt.
Beispiel, 30,9 Teile 4-Nitro-4'-amino-diphenylamin- 2-sulfosäure werden dianotiert und in soda- alkalischer Lösung mit 10,9 Teilen 3-Amino- 1-oxybenzol vereinigt. Nach beendigter Kupp lung werden noch 25 Teile Natriumcarbonat und eine Lösung von 50 Teilen kristallisier tem Kupfersulfat hinzugefügt und etwa eine Stunde unter Rückfluss gekocht oder längere Zeit, beispielsweise 2-3 Stunden, auf eine Temperatur von 70-80 erhitzt. Nach Fil tration wird der Farbstoff durch Zugabe von Chlornatrium abgeschieden.
Er färbt Chrom leder, sowie vegetabilisch gegerbtes Leder havannabraun.
proceed. for the production of an acid dye. It has been found that new, valuable dyes with the character of acid dyes are obtained by adding azo dyes, which are formed by alkaline coupling of 3-amino-1-oxybenzenes, their 4-position to the hydroxyl group is unoccupied;
are obtained with at least one solubilizing sulfonic or carboxylic acid group containing diazo compounds and do not contain a group capable of metal complex formation, treated in alkaline reading with oxidizing agents, preferably copper compounds. As a result, the azote taffies experience a change in their tone and an improvement in the lightfastness of the colorations achieved with them.
The present invention relates to a process for the production of such an acid dye, which is characterized in that the dye obtained from dianotated 4-nitro-4'-amino-diphenylamir2-sulfonic acid and 3-amino-1-oxybenzene in a soda-alkali solution is in alkaline solution treated with an oxidizing agent.
Example, 30.9 parts of 4-nitro-4'-aminodiphenylamine-2-sulfonic acid are dianotized and combined with 10.9 parts of 3-amino-1-oxybenzene in a soda-alkaline solution. After coupling is complete, 25 parts of sodium carbonate and a solution of 50 parts of crystallized copper sulfate are added and refluxed for about an hour or heated to a temperature of 70-80 for a longer period, for example 2-3 hours. After Fil tration, the dye is deposited by adding sodium chloride.
He dyes chrome leather and vegetable tanned leather havana brown.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE169692X | 1932-06-24 | ||
CH169692T | 1933-03-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH169692A true CH169692A (en) | 1934-06-15 |
Family
ID=25718753
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH169692D CH169692A (en) | 1932-06-24 | 1933-03-17 | Process for the preparation of an acid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH169692A (en) |
-
1933
- 1933-03-17 CH CH169692D patent/CH169692A/en unknown
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