CH231410A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH231410A CH231410A CH231410DA CH231410A CH 231410 A CH231410 A CH 231410A CH 231410D A CH231410D A CH 231410DA CH 231410 A CH231410 A CH 231410A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- azo dye
- new azo
- dye
- 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
Zusatzpatent zum Hauptpatent Nr. 229185. Verfahren zur Herstellung eines neuen Azofarbstofes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man das 2-Oxy-5'- methoxy-4'-aminoazobenzol mit Maleinsäure- anhydrid in der Aminogruppe acyliert.
Der neue Farbstoff bildet ein gelbes Pulver, das sich in Wasser mit gelber Farbe löst, und das Acetatkunstseide aus wässrigem 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 co-Methansulfonsäure des 1-Amino-2-me- thoxybenzols, Abspaltung der Toluolsulfon- säure und co-Methansulfonsäure, erhält, wer den in 200 Teilen Essigester mit 10,
8 Teilen Maleinsäureanhydrid während etwa 2 Stunden bei<B>70"</B> behandelt. Darnach wird Erkalten gelassen und der ausgefallene Farbstoff abfil- triert. Durch Trocknen; gegebenenfalls im Vakuum, wird von Essigester völlig befreit und hernach der Farbstoff mit etwa 500 Teilen reinem Wasser durch Zugabe eines Alkalis, z. B. Ammoniak, gelöst und durch Kochsalz das gebildete Ammoniumsalz des Farbstoffes vollständig ausgefällt, abfiltriert und getrocknet.
Additional patent 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 maleic anhydride in the amino group.
The new dye forms a yellow powder, which dissolves in water with a yellow color, and which dyes the acetate artificial silk from aqueous bath in real yellow tones.
Example: 24.3 parts of the 2-oxy-5'-methoxy-4'-amino-azobenzene, which is obtained by diazotizing the p-toluenesulfonic acid ester of 1-oxy-2-aminobenzene, coupling this diazo compound with the co-methanesulfonic acid of 1-amino-2-methoxybenzene, splitting off of toluenesulphonic acid and co-methanesulphonic acid, is obtained who in 200 parts of ethyl acetate with 10,
8 parts of maleic anhydride are treated for about 2 hours at <B> 70 "</B>. The mixture is then allowed to cool and the precipitated dye is filtered off. By drying, if necessary in vacuo, ethyl acetate is completely freed and then the dye with about 500 Partial pure water is dissolved by adding an alkali, e.g. ammonia, and the ammonium salt of the dye formed is completely precipitated with common salt, filtered off and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH231410T | 1942-07-02 | ||
CH229185T | 1942-07-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH231410A true CH231410A (en) | 1944-03-15 |
Family
ID=25727330
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH231410D CH231410A (en) | 1942-07-02 | 1942-07-02 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH231410A (en) |
-
1942
- 1942-07-02 CH CH231410D patent/CH231410A/en unknown
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