CH183893A - Process for the preparation of a dye. - Google Patents
Process for the preparation of a dye.Info
- Publication number
- CH183893A CH183893A CH183893DA CH183893A CH 183893 A CH183893 A CH 183893A CH 183893D A CH183893D A CH 183893DA CH 183893 A CH183893 A CH 183893A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- amino
- carboxylic acid
- preparation
- acid methyl
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Farbstoffes. Das Hauptpatent betrifft ein Verfahren zur Herstellung eines Farbstoffes, bei .dem 1- Amino - 4 - halog enanthrachinon - 2 - carbon - säuretaurid mit Anilin kondensiert wird.
Es wurde nun gefunden, dass man einen ähnlichen, ebenfalls sehr wertvollen Farb stoff erhält, wenn man 1-Amino-4-halogen- antlirachinon-2-carbonsäuremethyltaurid mit p-Aminoacetanilid kondensiert. Die Konden sation wird zweckmässig in Gegenwart von Wasser unter Zusatz von säurebindenden Mitteln und Katalysatoren ausgeführt.
Der erhaltene Farbstoff, das 1-Amino-4- (p - am inoacetanilino) - anthrachinon-2- earbon- säuremethyltaurid, färbt Wolle aus saurem Bade in grünstichig blauen Tönen.
Beispiel: 12 Teile 1-Amino-4-bromanthrachinon- ?- carbonsäuremethyltaurid ('erhältlich zum Bei spiel durch Kondensation von 1-Aminoanthra- chinon-2-carbonsäurechlorid mit 11'Iethyltaurin in alkalischer Lösung und Bromieren) werden in 100 Teilen Wasser mit 12 Teilen Natrium bicarbonat, 1 Teil Kupfersulfat und 20 Teilen p-Aminoacetanilid so lange auf 70 C er hitzt, bis die Farbstoffbildung beendet ist. Nach dem Erkalten saugt man den gebildeten Farbstoff ab.
Process for the preparation of a dye. The main patent relates to a process for the production of a dye in which 1-amino-4-halo-enanthraquinone-2-carboxylic acid tauride is condensed with aniline.
It has now been found that a similar, also very valuable dye is obtained if 1-amino-4-halo-antlirachinone-2-carboxylic acid methyl tauride is condensed with p-aminoacetanilide. The condensation is expediently carried out in the presence of water with the addition of acid-binding agents and catalysts.
The dye obtained, 1-amino-4- (p - am inoacetanilino) - anthraquinone-2-earbonic acid methyltauride, dyes wool from an acid bath in greenish blue shades.
Example: 12 parts of 1-amino-4-bromoanthraquinone? - carboxylic acid methyl tauride ('obtainable for example by condensation of 1-aminoanthraquinone-2-carboxylic acid chloride with 11'-ethyltaurine in an alkaline solution and bromination) are added to 100 parts of water with 12 Parts of sodium bicarbonate, 1 part of copper sulfate and 20 parts of p-aminoacetanilide are heated to 70 C until the dye has formed. After cooling, the dye formed is filtered off with suction.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE183893X | 1933-01-21 | ||
CH178226T | 1933-12-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH183893A true CH183893A (en) | 1936-04-30 |
Family
ID=25720100
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH183893D CH183893A (en) | 1933-01-21 | 1933-12-20 | Process for the preparation of a dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH183893A (en) |
-
1933
- 1933-12-20 CH CH183893D patent/CH183893A/en unknown
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