CH187923A - Process for the preparation of an insoluble azo dye. - Google Patents
Process for the preparation of an insoluble azo dye.Info
- Publication number
- CH187923A CH187923A CH187923DA CH187923A CH 187923 A CH187923 A CH 187923A CH 187923D A CH187923D A CH 187923DA CH 187923 A CH187923 A CH 187923A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- insoluble azo
- preparation
- diazotized
- dye
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines unlöslichen Azofarbstoffes. Gemäss dem im Hauptpatent beschrie benen Verfahren erhält man einen Acetat seide in blaustichig roten Tönen anfärbenden unlöslichen Azofarbstoff, wenn man 4-Ni- tro-l-aminoben.zol diazotiert und die Diazo- verbindung mit 1-Butyl-3-oxy-7-chlortetra- liydroehinolin kuppelt.
Wie nun weiter gefunden wurde, erhält man einen Farbstoff von ähnlichen Eigen schaften, wenn man 6-Brom-2.4-dinitro-l- aminobenzol diazotiert und die Diazoverbin- dung mit 1-Äthyl-3-oxy-7-methyl-tetrahydro- chinolin kuppelt.
<I>Beispiel:</I> 26,2 Teile 6-Brom-2. 4-dinitro-l-amino- benzol werden in der üblichen Weise diazo- 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 ein laufen 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-1-aminoben.zol is diazotized and the diazo compound is treated with 1-butyl-3-oxy-7- chlorotetra- liydroehinoline couples.
As has now been found further, a dye with similar properties is obtained if 6-bromo-2,4-dinitro-l-aminobenzene is diazotized and the diazo compound is diazotized with 1-ethyl-3-oxy-7-methyl-tetrahydroquinoline clutch.
<I> Example: </I> 26.2 parts 6-bromo-2. 4-Dinitro-1-aminobenzene are diazotized in the usual way. The diazo compound is poured 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 terminate 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 |
---|---|---|---|
DE187923X | 1934-08-11 | ||
CH185944T | 1935-05-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH187923A true CH187923A (en) | 1936-11-30 |
Family
ID=25721284
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH187923D CH187923A (en) | 1934-08-11 | 1935-05-07 | Process for the preparation of an insoluble azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH187923A (en) |
-
1935
- 1935-05-07 CH CH187923D patent/CH187923A/en unknown
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