CH188773A - Process for the preparation of an insoluble azo dye. - Google Patents
Process for the preparation of an insoluble azo dye.Info
- Publication number
- CH188773A CH188773A CH188773DA CH188773A CH 188773 A CH188773 A CH 188773A CH 188773D A CH188773D A CH 188773DA CH 188773 A CH188773 A CH 188773A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- insoluble azo
- dye
- aminobenzene
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines unlöslichen .A zofarbstoifes. Gemäss dem im Hauptpatent beschriebe neu 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-oxy- 7- chlortetrahydro- chinolin kuppelt.
Wie nun weiter gefunden wurde, erhält man einen Farbstoff von ähnlichen Eigen schaften, wenn man 4-Nitro-2-chlor-l-amino- benzol diazotiert und die Diazoverbindung mit 1-Benzyl-3-oxy-tetrahydrochinolin kup pelt.
<I>Beispiel:</I> 17,3 Teile 4-Nitro-2-chlor-l-aminobenzol werden in der üblichen Weise diazotiert. Die Diazoverbindung lässt man in eine eisgekühlte Lösung von 23,9 Teilen 1-Benzyl-3-oxy-tetra- hydrochinolin in der entsprechenden Menge verdünnter Salzsäure einlaufen und stumpft zur Beendigung der Kupplung mit Natrium acetat ab. Der erhaltene Farbstoff -färbt Acetatseide im Seifensuspensionsbad bordo.
Process for the preparation of an insoluble .A zofarbstoifes. According to the new 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-oxy-7-chlorotetrahydroquinoline .
As has now been found further, a dye with similar properties is obtained if 4-nitro-2-chloro-1-aminobenzene is diazotized and the diazo compound is coupled with 1-benzyl-3-oxy-tetrahydroquinoline.
<I> Example: </I> 17.3 parts of 4-nitro-2-chloro-1-aminobenzene are diazotized in the usual way. The diazo compound is allowed to run into an ice-cold solution of 23.9 parts of 1-benzyl-3-oxy-tetrahydroquinoline in the appropriate amount of dilute hydrochloric acid and blunted with sodium acetate to complete the coupling. The dye obtained dyes acetate silk in a bordo soap suspension bath.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE188773X | 1934-08-11 | ||
CH185944T | 1935-05-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH188773A true CH188773A (en) | 1937-01-15 |
Family
ID=25721288
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH188773D CH188773A (en) | 1934-08-11 | 1935-05-07 | Process for the preparation of an insoluble azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH188773A (en) |
-
1935
- 1935-05-07 CH CH188773D patent/CH188773A/en unknown
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