CH209553A - Process for the preparation of a new derivative of an azo dye. - Google Patents
Process for the preparation of a new derivative of an azo dye.Info
- Publication number
- CH209553A CH209553A CH209553DA CH209553A CH 209553 A CH209553 A CH 209553A CH 209553D A CH209553D A CH 209553DA CH 209553 A CH209553 A CH 209553A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- new derivative
- 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. 205164. Verfahren zur Herstellung eines neuen Derivates eines Azofarbstoffes. Es wurde gefunden, dass man ein neues Derivat eines Azofarbstoffes erhält, wenn man<B>1</B> Mol des Monoazofarbstoffes, der er halten wird durch Vereinigen eines Moleküls des 1,3-Diamitibenzols mit<B>1</B> Mol der diazo- tierten Anilin-2,5-disulfonsäure,
mit 2 Mol Acetyleblorid in Gegenwart einer tertiären Base acyliert.
Der neue Farbstoff stellt ein orangerotes Pulver dar und färbt Wolle in echten gelben Tönen.
<I>Beispiel:</I> <B>1</B> Teil des Monoazofarbstoffes, der er halten wird durch Vereinigen von 1,3-Di- aminobenzol. mit der diazotierten Anilin-2,5- disulfonsäure, wird in<B>6,7</B> Teilen Pyridin suspendiert und bei 400 mit<B>1,25</B> Teilen Acetylchlorid versetzt. Man erwärmt allmäh- lieh auf<B>900</B> und hält diese Temperatur <B>1</B>1/2 Stunden. Nach dieser Zeit wird das Di- acetylprodukt abgeschieden und getrocknet.
Additional patent to main patent no. 205164. Process for the production of a new derivative of an azo dye. It has been found that a new derivative of an azo dye is obtained by adding <B> 1 </B> moles of the monoazo dye obtained by combining one molecule of 1,3-diamitibenzene with <B> 1 </B> Mol of the diazo-aniline-2,5-disulfonic acid,
acylated with 2 moles of acetyl chloride in the presence of a tertiary base.
The new dye is an orange-red powder and dyes wool in real yellow tones.
<I> Example: </I> <B> 1 </B> Part of the monoazo dye that is obtained by combining 1,3-diaminobenzene. with the diazotized aniline-2,5-disulfonic acid, is suspended in 6.7 parts of pyridine and, at 400, 1.25 parts of acetyl chloride are added. It is gradually heated to <B> 900 </B> and this temperature is maintained for <B> 1 </B> 1/2 hours. After this time, the di-acetyl product is separated out and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH209553T | 1937-01-26 | ||
CH205164T | 1939-02-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH209553A true CH209553A (en) | 1940-04-15 |
Family
ID=25724140
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH209553D CH209553A (en) | 1937-01-26 | 1937-01-26 | Process for the preparation of a new derivative of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH209553A (en) |
-
1937
- 1937-01-26 CH CH209553D patent/CH209553A/en unknown
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