CH188774A - Process for the preparation of an insoluble azo dye. - Google Patents
Process for the preparation of an insoluble azo dye.Info
- Publication number
- CH188774A CH188774A CH188774DA CH188774A CH 188774 A CH188774 A CH 188774A CH 188774D A CH188774D A CH 188774DA CH 188774 A CH188774 A CH 188774A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- insoluble azo
- preparation
- dye
- oxy
- Prior art date
Links
Landscapes
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines unlöslichen Azofarbstof%s. 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-oxy-7-chlortetrahydro- chinolin kuppelt.
Wie nun weiter gefunden wurde, erhält man einen Farbstoff von ähnlichen Eigen schaften, wenn man 2. 6-Dichlor-l-amino-4- nitrobenzol diazotiert und die Diazoverbin- dung mit 1-Benzyl-3-oxy-tetrahydrochinolin kuppelt.
<I>Beispiel:</I> 20,7 Teile 2.6-Dichlor-l-amino-4-nitro- benzol werden in der üblichen Weise diazo- tiert. Die Diazoverbindung lässt man in eine eisgekühlte Lösung von 23,9 Teilen 1-Ben- zyl-3-oxy-tetrahydrochinolin in der entspre chenden Menge verdünnter Salzsäure einlau fen und stumpft zur Beendigung der Kupp- lung mit Natriumacetat ab.
Der erhaltene Farbstoff färbt Acetatseide im Seifensuspen- sionsbad blaustichig braun.
Process for the preparation of an insoluble azo dye% s. 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 obtained with 1-butyl-3-oxy-7-chlorotetrahydroquinoline clutch.
As has now also been found, a dye with similar properties is obtained if 2. 6-dichloro-1-amino-4-nitrobenzene is diazotized and the diazo compound is coupled with 1-benzyl-3-oxy-tetrahydroquinoline.
<I> Example: </I> 20.7 parts of 2,6-dichloro-1-amino-4-nitrobenzene are diazo- tated 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 terminate the coupling.
The dye obtained dyes acetate silk in the soap suspension bath with a bluish brown tinge.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE188774X | 1934-08-11 | ||
CH185944T | 1935-05-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH188774A true CH188774A (en) | 1937-01-15 |
Family
ID=25721289
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH188774D CH188774A (en) | 1934-08-11 | 1935-05-07 | Process for the preparation of an insoluble azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH188774A (en) |
-
1935
- 1935-05-07 CH CH188774D patent/CH188774A/en unknown
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