CH249014A - Process for the preparation of an ester type azo dye derivative. - Google Patents
Process for the preparation of an ester type azo dye derivative.Info
- Publication number
- CH249014A CH249014A CH249014DA CH249014A CH 249014 A CH249014 A CH 249014A CH 249014D A CH249014D A CH 249014DA CH 249014 A CH249014 A CH 249014A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- dye derivative
- ester type
- oxy
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines esterartigen Azofarbstoffderivates. Gegenstand des. vorliegenden Zusatzpaten tes ist ein Verfahren zur Herstellung eines esterartigen Derivates eines o,ö -Dioxyazo- farbstoffes, dadurch gekennzeichnet, dass der Azofarbstoff aus diazotiertem 1 - Oxy - 2 - amino-4-chlor-5-nitrobenzol und 1-Oxy-5,
8- dichlornaphtalin in Gegenwart von Pyridin mit Benzoesäure - 3 - sulfochlorid verestert wird.
Das neue Farbstoffderivat bildet nach dem Aufarbeiten und Trocknen ein braunes, wasserlösliches Pulver. Es färbt Wolle nach dem Einbadverfahren in Gegenwart chrom abgebender Mittel in blaugrünen Tönen. Beispiel: 66 Teile Benzoesäure-3-sulfochlorid wer den in 270 Teilen Pyridin bei 50 bis 60 gelöst.
Bei 40 bis. 50 werden 41,2 Teile des Azofarbstoffes aus diazotiertem 1 - Oxy - 2 - amino-4-chlor-5-nitrobenzol und 1-Oxy-5,8- diehlornaphtalin unter gutem Rühren zu gegeben. Nach zwei Stunden ist .die Vereste- rung beendet.
Dann wird das Pyridin im Vakuum abdestilliert, der Destillationsrück- sta.nd in etwa 500 Teilen Wasser aufgenom men und der Farbstoffester mit 100 Teilen Natriumchlorid ausgesalzen. Die Masse wird verrührt, bis das Farbstoffderivat ,gut fil- trierbar geworden ist. Hierauf wird ab filtriert und im Vakuum getrocknet.
Process for the preparation of an ester type azo dye derivative. The subject of the present additional patent is a process for the preparation of an ester-like derivative of an o, o -dioxyazo dye, characterized in that the azo dye is made from diazotized 1-oxy-2-amino-4-chloro-5-nitrobenzene and 1-oxy -5,
8-dichloronaphthalene is esterified with benzoic acid - 3 - sulfochloride in the presence of pyridine.
After working up and drying, the new dye derivative forms a brown, water-soluble powder. It dyes wool by the single bath process in the presence of chromium-releasing agents in blue-green tones. Example: 66 parts of benzoic acid 3-sulfochloride who dissolved in 270 parts of pyridine at 50 to 60.
At 40 to. 50 41.2 parts of the azo dye from diazotized 1-oxy-2-amino-4-chloro-5-nitrobenzene and 1-oxy-5,8-diehlornaphthalene are added with thorough stirring. The esterification is over after two hours.
The pyridine is then distilled off in vacuo, the distillation residue is taken up in about 500 parts of water and the dye ester is salted out with 100 parts of sodium chloride. The mass is stirred until the dye derivative has become easy to filter. It is then filtered off and dried in vacuo.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH249014T | 1944-10-06 | ||
CH244049T | 1945-08-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH249014A true CH249014A (en) | 1947-05-31 |
Family
ID=25728868
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH249014D CH249014A (en) | 1944-10-06 | 1944-10-06 | Process for the preparation of an ester type azo dye derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH249014A (en) |
-
1944
- 1944-10-06 CH CH249014D patent/CH249014A/en unknown
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