CH187924A - Process for the preparation of an insoluble azo dye. - Google Patents
Process for the preparation of an insoluble azo dye.Info
- Publication number
- CH187924A CH187924A CH187924DA CH187924A CH 187924 A CH187924 A CH 187924A CH 187924D A CH187924D A CH 187924DA CH 187924 A CH187924 A CH 187924A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- insoluble azo
- dye
- oxy
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines unlöslichen Azofarbstoffes. Gemäss dem im Hauptpatent beschriebenen Verfahren erhält man einen Acetatseide in blaustichig roten Tönen anfärbenden unlös lichen Azofarbstoff, wenn man 4-Nitro-l- aminobenzol dianotiert und die Diazoverbin- dung mit 1-Butyl-3-oxy-7-chlortetrabydrochi- nolin kuppelt.
Wie nun weiter gefunden wurde, erhält man einen Farbstoff von ähnlichen Eigen schaften, wenn man 6-Chlor-2.4-dinitro-l- aminobenzol dianotiert und die Diazoverbin- dung mit 1-Äthyl-3-oxy-7-methyl-tetrahydro- chinolin kuppelt.
<I>Beispiel:</I> 21,8 Teile 6-Chlor-2.4-dinitro-l-amino- benzol werden in der üblichen Weise diano tiert. Die Diazoverbindung lässt man in eine eisgekühlte Lösung von 19,2 Teilen 1-Äthyl- 3-oxy-7-methyl-tetrahydrochinolin in der ent sprechenden Menge verdünnter Salzsäure einlaufen und stumpft zur Beendigung der Kupplung mit Natriumacetat ab. Der erhal tene Farbstoff färbt Acetatseide im Seifen suspensionsbad rötlich blau.
Process for the preparation of an insoluble azo dye. According to the process described in the main patent, an insoluble azo dye which stains acetate silk in bluish red shades is obtained if 4-nitro-l-aminobenzene is dianotated and the diazo compound is coupled with 1-butyl-3-oxy-7-chlorotetrabydroquinoline.
As has now been found further, a dye with similar properties is obtained if 6-chloro-2,4-dinitro-l-aminobenzene is dianotized and the diazo compound is dianotated with 1-ethyl-3-oxy-7-methyl-tetrahydroquinoline clutch.
<I> Example: </I> 21.8 parts of 6-chloro-2,4-dinitro-1-amino-benzene are diano-benefits in the usual way. The diazo compound is allowed to run into an ice-cold solution of 19.2 parts of 1-ethyl-3-oxy-7-methyl-tetrahydroquinoline in the appropriate amount of dilute hydrochloric acid and blunted with sodium acetate to complete the coupling. The dye obtained gives the acetate silk a reddish blue color in the soap suspension bath.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE187924X | 1934-08-11 | ||
CH185944T | 1935-05-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH187924A true CH187924A (en) | 1936-11-30 |
Family
ID=25721285
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH187924D CH187924A (en) | 1934-08-11 | 1935-05-07 | Process for the preparation of an insoluble azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH187924A (en) |
-
1935
- 1935-05-07 CH CH187924D patent/CH187924A/en unknown
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