CH121708A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH121708A CH121708A CH121708DA CH121708A CH 121708 A CH121708 A CH 121708A CH 121708D A CH121708D A CH 121708DA CH 121708 A CH121708 A CH 121708A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- dye
- weight
- parts
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Description
Verfahren zur Darstellung eines Azofarbstoifes. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung eines Azofarb- stoffes aus 4(p-Toluolsulfonmethylamino)-1- methoxy-2-aminobenzol und 2-Oxynaphtalin- 3-karbonsäure-5'-chlor-2'-methoxyanilid.
<I>Beispiel:</I> 6.12 Gewichtsteile 4 - (p - Toluolsulfon- methylarnino)-1-methoxy-2-aminobenzol wer den gelöst in etwa 50 Gewichtsteilen Wasser und 7 (xewichtsteilen Salzsäure 20 B6 und mit 1,4 Gewichtsteilen. Natriumnitrit diazotiert.
Die Diazoverbindung wird vereinigt mit einer Auflösung von 7.2 Gewichtsteilen 2- Oxynaphtalin - 3 -karbonsäure - 5'- chlor-2'-me- thoxyanilid in etwa 400 Gewichtsteilen Was ser und 10 Gewichtsteilen Natronlauge von 40 B6. Es entsteht ein bordeauxroter Nieder schlag, der abfiltriert und getrocknet werden kann.
Der Farbstoff ist ein bordeauxrotes Pulver, das sich in konzentrierter Schwefelsäure mit blauroter Farbe löst.
Process for the preparation of an azo dye. The subject of this additional patent is a process for the preparation of an azo dye from 4 (p-toluenesulfonmethylamino) -1-methoxy-2-aminobenzene and 2-oxynaphthalene-3-carboxylic acid 5'-chloro-2'-methoxyanilide.
<I> Example: </I> 6.12 parts by weight of 4 - (p - toluenesulfonemethylamino) -1-methoxy-2-aminobenzene are dissolved in about 50 parts by weight of water and 7 (x parts by weight of hydrochloric acid 20 B6 and 1.4 parts by weight. Sodium nitrite diazotized.
The diazo compound is combined with a dissolution of 7.2 parts by weight of 2-oxynaphthalene - 3 -carboxylic acid - 5'-chloro-2'-methoxyanilide in about 400 parts by weight of water and 10 parts by weight of 40 B6 sodium hydroxide solution. A burgundy precipitate is formed, which can be filtered off and dried.
The dye is a burgundy red powder that dissolves in concentrated sulfuric acid with a blue-red color.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH114916T | 1925-03-24 | ||
DE121708X | 1925-07-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH121708A true CH121708A (en) | 1927-07-16 |
Family
ID=25708423
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH121708D CH121708A (en) | 1925-03-24 | 1926-07-22 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH121708A (en) |
-
1926
- 1926-07-22 CH CH121708D patent/CH121708A/en unknown
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