CH130331A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH130331A CH130331A CH130331DA CH130331A CH 130331 A CH130331 A CH 130331A CH 130331D A CH130331D A CH 130331DA CH 130331 A CH130331 A CH 130331A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- dye
- anilide
- chlorobenzene
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Azofarbstoffes. Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Darstellung eines Azo- farbstoffes, den man durch Kupplung der Diazoverbindung von 1,3,6 - Trimethyl- 4 - amino-2-chlorbenzol mit 2-Ogynaphtalin-3- earbonsäure-4'-chlor-2'-methyl-1'-anilid er hält.
<I>Beispiel:</I> Die aus 17 kg 1,3,6-Trimethyl-4-amino- 2-chlorbenzol in üblicher Weise dargestellte Dia.zoverbindung lässt man unter Rühren in eine wässerige Suspension von 31 kg 2-Oxy- naphtalin- 3 -.carbonsäure-4'-chlor- 2'-methyl- 1'-anilid, bereitet durch Auflösen desselben in Natronlauge und Wiederausfällen mit verdünnter Essigsäure, einlaufen. Der Farb stoff scheidet sich als roter Niederschlag aus.
Er wird filtriert, gewaschen und getrocknet.
Der Farbstoff soll besonders als Ent wicklungsfarbstoff verwendet werden. Er hat eine klare Rotnuance und besitzt die wichtige Eigenschaft, dass er zur Erzeugung von gut lichtechten und hervorragend laugen kochechten, klaren Rottönen idienen kann.
Process for the preparation of an azo dye. The present invention is a process for the preparation of an azo dye, which can be obtained by coupling the diazo compound of 1,3,6-trimethyl-4-amino-2-chlorobenzene with 2-ogynaphthalene-3-carboxylic acid-4'-chloro He holds 2'-methyl-1'-anilide.
<I> Example: </I> The dia.zo compound prepared in the usual way from 17 kg of 1,3,6-trimethyl-4-amino-2-chlorobenzene is allowed to stir in an aqueous suspension of 31 kg of 2-oxy- naphthalene-3-carboxylic acid-4'-chloro-2'-methyl-1'-anilide, prepared by dissolving it in sodium hydroxide solution and reprecipitating it with dilute acetic acid, run in. The dye separates out as a red precipitate.
It is filtered, washed and dried.
The dye should be used especially as a development dye. It has a clear nuance of red and has the important property that it can be used to produce clear red tones that are good lightfast and excellent caustic, boil-fast.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE130331X | 1926-08-05 | ||
CH127528T | 1927-07-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH130331A true CH130331A (en) | 1928-11-30 |
Family
ID=25710910
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH130331D CH130331A (en) | 1926-08-05 | 1927-07-08 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH130331A (en) |
-
1927
- 1927-07-08 CH CH130331D patent/CH130331A/en unknown
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