CH188772A - Process for the preparation of an insoluble azo dye. - Google Patents
Process for the preparation of an insoluble azo dye.Info
- Publication number
- CH188772A CH188772A CH188772DA CH188772A CH 188772 A CH188772 A CH 188772A CH 188772D A CH188772D A CH 188772DA CH 188772 A CH188772 A CH 188772A
- 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 Azofarbstofes. 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 4-Nitro-l-äminobenzol diazotiert und die Diazoverbindung mit 1- Benzyl - 3 - oxy - 7 - methyl -tetrahydrochinolin kuppelt.
<I>Beispiel:</I> 13,8 Teile 4-Nitro-l-aminobenzol werden in der üblichen Weise diazotiert. Die Diazo- verbindung lässt man in eine eisgekühlte Lö sung von 2.5,3 Teilen 1-Benzyl-3-ogy-7- methyl-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 rubinrot.
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-oxy-7-chlorotetrahydroquinoline .
As has now been found further, a dye with similar properties is obtained if 4-nitro-1-aminobenzene is diazotized and the diazo compound is coupled with 1-benzyl - 3 - oxy - 7 - methyl tetrahydroquinoline.
<I> Example: </I> 13.8 parts of 4-nitro-1-aminobenzene are diazotized in the usual way. The diazo compound is allowed to run into an ice-cold solution of 2.5.3 parts of 1-benzyl-3-ogy-7-methyl-tetrahydroquinoline in the appropriate amount of dilute hydrochloric acid; and dulls to terminate the coupling with sodium acetate.
The dye obtained dyes acetate silk ruby red in the soap suspension bath.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE188772X | 1934-08-11 | ||
CH185944T | 1935-05-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH188772A true CH188772A (en) | 1937-01-15 |
Family
ID=25721287
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH188772D CH188772A (en) | 1934-08-11 | 1935-05-07 | Process for the preparation of an insoluble azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH188772A (en) |
-
1935
- 1935-05-07 CH CH188772D patent/CH188772A/en unknown
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