CH231409A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH231409A CH231409A CH231409DA CH231409A CH 231409 A CH231409 A CH 231409A CH 231409D A CH231409D A CH 231409DA CH 231409 A CH231409 A CH 231409A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- production
- new azo
- yellow
- new
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 229185. Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man das 2-Oxy-5'- methoxy-4'-aminoazobenzol mit Phthalsäure- anhydrid in der Aminogruppe acyliert.
<B>S</B> Der neue Farbstoff bildet ein gelbbraunes Pulver, das sich in Wasser mit gelber Farbe löst und das Acetatkunstseide aus- wässerigem Bade in echten gelben Tönen färbt.
Beispiel: 24,3 Teile des 2-Oxy-5'-methoxy-4'-amino- azobenzols, das man durch Diazotieren des p-Toluolsulfonsäureesters des 1-Oxy-2-amino- benzols, Kuppeln dieser Diazoverbindung mit der ai-Methansulfonsäure des 1-Amino-2-meth- oxybenzols, Abspaltung der Toluolsulfonsäure, und der oo-Methansulfonsäure, erhält, werden in 300 Teilen Chlorbenzol mit 16,
3 Teilen Phthalsäureanhydrid während etwa 18 Stun den bei 50-60 behandelt. Darnach wird er kalten gelassen und der ausgefallene Farb stoff abfiltriert. Durch Trocknen, gegebenen- falls im Vakuum, wird von Chlorbenzol völlig befreit und hernach der Farbstoff mit etwa 500 Teilen reinem Wasser verrührt und durch Zugabe eines Alkalis, z. B. Ammoniak, neu tralisiert. Dann wird das gebildete Ammo- niumsalz des Farbstoffes, gegebenenfalls durch Zusatz eines Salzes, vollständig ausgefällt, abfiltriert und getrocknet.
<B> Additional patent </B> to main patent no. 229185. Process for the production of a new azo dye. It has been found that a new azo dye is obtained if the 2-oxy-5'-methoxy-4'-aminoazobenzene is acylated with phthalic anhydride in the amino group.
<B> S </B> The new dye forms a yellow-brown powder, which dissolves in water with a yellow color and colors the acetate artificial silk in real yellow tones when bathed in water.
Example: 24.3 parts of 2-oxy-5'-methoxy-4'-amino-azobenzene, which is obtained by diazotizing the p-toluenesulphonic acid ester of 1-oxy-2-aminobenzene, coupling this diazo compound with the ai-methanesulphonic acid of 1-amino-2-methoxybenzene, splitting off of toluenesulfonic acid, and oo-methanesulfonic acid, are obtained in 300 parts of chlorobenzene with 16,
3 parts of phthalic anhydride treated at 50-60 for about 18 hours. It is then left cold and the precipitated dye is filtered off. Chlorobenzene is completely removed by drying, if necessary in vacuo, and the dye is then stirred with about 500 parts of pure water and treated by adding an alkali, e.g. B. ammonia, neutralized. The ammonium salt of the dye that is formed is then completely precipitated, filtered off and dried, if appropriate by adding a salt.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH229185T | 1942-07-02 | ||
CH231409T | 1942-07-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH231409A true CH231409A (en) | 1944-03-15 |
Family
ID=25727329
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH231409D CH231409A (en) | 1942-07-02 | 1942-07-02 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH231409A (en) |
-
1942
- 1942-07-02 CH CH231409D patent/CH231409A/en unknown
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