CH189800A - Process for the preparation of an insoluble azo dye. - Google Patents
Process for the preparation of an insoluble azo dye.Info
- Publication number
- CH189800A CH189800A CH189800DA CH189800A CH 189800 A CH189800 A CH 189800A CH 189800D A CH189800D A CH 189800DA CH 189800 A CH189800 A CH 189800A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- insoluble azo
- preparation
- dye
- aminobenzene
- Prior art date
Links
Landscapes
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines unlöslichen Azofarbstoffes. Gemäss dem im Hauptpatent beschriebe nen Verfahren erhält man einen Acetatseide in blaustichig roten Tönen anfärbenden un löslichen Azofarbstoff, wenn man 4-Nitro-l- aminobenzol diazotiert und die Diazoverbin- dung mit 1-Butyl-3-ogy-7-chlortetrahydrochi- nolin kuppelt.
Wie nun weiter gefunden wurde, erhält man einen Farbstoff von ähnlichen Eigen schaften, wenn man 4-Nitro-l-aminobenzol diazotiert und die Diazoverbindung mit 1-sec. Butyl-'3-oxy-7-methyltetrahydrochino- lin kuppelt.
<I>Beispiel:</I> Eine Diazolösung, welche bereitet wurde aus 13,S Teilen 4-Nitro-l-aminobenzol, lässt man einfliessen in eine kalte Lösung von 21,9 Teilen 1-sec.Butyl-3-oxy-7-methyltetrahydro- chinolin in 20 Teilen Salzsäure 23' B6 und 800 Teilen Wasser und stumpft zur Beendi gung der Kupplung mit Natriumacetat ab. Der erhaltene Farbstoff färbt Acetats,eide in klaren blauen; Bordotönen an.
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 diazotized and the diazo compound is coupled with 1-butyl-3-ogy-7-chlorotetrahydroquinoline .
As has now been found further, a dye of similar properties is obtained if 4-nitro-l-aminobenzene is diazotized and the diazo compound with 1 sec. Butyl-3-oxy-7-methyltetrahydroquinoline couples.
<I> Example: </I> A diazo solution, which was prepared from 13.5 parts of 4-nitro-l-aminobenzene, is allowed to flow into a cold solution of 21.9 parts of 1-sec-butyl-3-oxy- 7-methyltetrahydroquinoline in 20 parts of hydrochloric acid 23 'B6 and 800 parts of water and is blunted to complete the coupling with sodium acetate. The dye obtained stains acetate, both in clear blue; Bordo tones on.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE189800X | 1934-08-11 | ||
CH185944T | 1935-05-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH189800A true CH189800A (en) | 1937-03-15 |
Family
ID=25721297
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH189800D CH189800A (en) | 1934-08-11 | 1935-05-07 | Process for the preparation of an insoluble azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH189800A (en) |
-
1935
- 1935-05-07 CH CH189800D patent/CH189800A/en unknown
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