CH107620A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH107620A CH107620A CH107620DA CH107620A CH 107620 A CH107620 A CH 107620A CH 107620D A CH107620D A CH 107620DA CH 107620 A CH107620 A CH 107620A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- dye
- acid
- toluidide
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Azofarbstoffes. Es wurde gefunden. dass man zu einem Farbstoff, welcher Färbungen von ausge zeichneten Echtheitseigenschaften, gibt, ge langt, wenn man die Diazoverbindung von m-Ami,do-p-methoxybenzoesäure-anilid mit 2 - 3 - oxy naphtoesäure - 5 - chlor - 2 - toluidid (CH:, : NI-I2 : Cl = 1 : 2 : 5) kuppelt. Man erhält: hierbei einen Farbstoff von ausge zeichnet klarer, blaustichig roter Nuance.
der die wichtige Eigenschaft besitzt, dass er zur Erzeugung von echten alizarinrosa Tönen dienen kann.
Beispiel: Die aus<U>94,2-</U> kg Metaamidopara.methoxy- benzoesäureanilid in üblicher Weise darge stellte Diazoverbindung lässt man unter Rühren in eine wiisserige Suspension von . 31 kg 2 - 3-oxynaphtoesäure-5-chlor-2-toluidid (CHF : NH, : Cl === 1 : 2 : 5), bereitet durch Auflösen desselben in Natronlauge und 'Wie- clerausfällen mit verdünnter Essigsäure, ein laufen.
Der Farbstoff scheidet sich als roter Niederschlag aus. Darauf wird filtriert; ge waschen und getrocknet.
Process for the preparation of an azo dye. It was found. that one arrives at a dye which gives dyeings with excellent fastness properties if one uses the diazo compound of m-ami, do-p-methoxybenzoic acid anilide with 2 - 3 - oxy naphthoic acid - 5 - chloro - 2 - toluidide ( CH :,: NI-I2: Cl = 1: 2: 5) couples. The following is obtained: a dye with an excellent clear, bluish red shade.
which has the important property that it can be used to create real alizarin pink tones.
Example: The diazo compound prepared in the usual way from <U> 94.2 </U> kg of metaamidopara.methoxybenzoic acid anilide is allowed to stir into an aqueous suspension of. 31 kg of 2- 3-oxynaphthoic acid-5-chloro-2-toluidide (CHF: NH,: Cl === 1: 2: 5), prepared by dissolving it in sodium hydroxide solution and precipitating it again with dilute acetic acid.
The dye separates out as a red precipitate. It is then filtered; ge wash and dry.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE107620X | 1923-01-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH107620A true CH107620A (en) | 1924-11-01 |
Family
ID=5651064
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH107620D CH107620A (en) | 1923-01-18 | 1924-01-15 | Process for the preparation of an azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH107620A (en) |
-
1924
- 1924-01-15 CH CH107620D patent/CH107620A/en unknown
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