CH220650A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH220650A CH220650A CH220650DA CH220650A CH 220650 A CH220650 A CH 220650A CH 220650D A CH220650D A CH 220650DA CH 220650 A CH220650 A CH 220650A
- Authority
- CH
- Switzerland
- Prior art keywords
- mole
- amino
- production
- new
- product
- 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
- C09B43/136—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
- C09B43/16—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents linking amino-azo or cyanuric acid residues
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 217241. Verfahren zur Herstellung eines neuen AzofarbstofFes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man 1 Mol Cyanurchlorid, 1 Mol der 1-Amino-4-(4'- amino- 3'-sulf o)-anilidoanthrachinon-2-sulf on- säure, 1 Mol des Produktes,
das erhalten wird durch Reduzieren .des A.cylierungs- produktes aus 1 Mol meta-Nitrobenzoylchlo- rid und 1 Mol 4-Amino-4'-ogy-1,1'-azobenzol- 3'-carbonsäure und 1 Mol Anilin aufeinander einwirken lässt.
Der neue Farbstoff stellt ein dunkles Pulver .dar, das sich in Wasser mit grüner Farbe löst und Baumwolle in schwach alkalischem Bade in Gegenwart von Kupfer sulfat und weinsaurem Natrium in wasch- und lichtechten grünen Tönen färbt.
<I>Beispiel:</I> 48,'9 Gewichtsteile 1-Amino-4-(4'-amino- 3' - sulfo) - anilidoanthraehinon -'2 -sulfonsäure werden als neutrale Lösung in 1000 Ge- wichtsteilen Wasser zu einer Anschlämmung von 18.5 Gewichtsteilen Cyanurchlorid in 500 Gewichtsteilen kaltem Wasser gegeben. Man hält die Temperatur 4 ,Stunden bei 10 bis 15 .
Die bei der Kondensation ent stehende Salzsäure wird durch die entspre chende Menge Natriumcarbonat neutralisiert. Hernach werden 37;
6 Gewichtsteile Jes Pro duktes, das erhalten wird durch Reduzieren des Acylierungsproduktes aus meta-Nitro- benzoylchlorid und 4-Amino-4'-ogy-1,1'-azo- benzol-,3'-carbonsäure in 50,0 Gewichtsteilen warmem Wasser gelöst, zum Monokondeiuea- tionsprodukt .gegeben. Die Temperatur wird dabei auf 40 erhöht.
Nach 24 Stunden .gibt man 18 Gewichtsteile Anilin zu und hält die Temperatur während der ,gleichen Zeit auf 80 . Das tertiäre Kondensationsprodukt ist nach dieser Zeit .gebildet, Es wird mit Na- triumehlorid abgeschieden und getrocknet.
<B> Additional patent </B> to main patent no. 217241. Process for the production of a new azo dye. It has been found that a new azo dye is obtained when 1 mole of cyanuric chloride, 1 mole of 1-amino-4- (4'-amino-3'-sulfo) -anilidoanthraquinone-2-sulfonic acid, 1 mole of the product,
this is obtained by reducing the acylation product from 1 mole of meta-nitrobenzoyl chloride and 1 mole of 4-amino-4'-ogy-1,1'-azobenzene-3'-carboxylic acid and 1 mole of aniline .
The new dye is a dark powder that dissolves in water with a green color and colors cotton in a weakly alkaline bath in the presence of copper sulfate and tartrate of sodium in washable and lightfast green tones.
<I> Example: </I> 48, '9 parts by weight of 1-amino-4- (4'-amino-3' - sulfo) - anilidoanthraehinone -'2 -sulfonic acid become a neutral solution in 1000 parts by weight of water Added suspension of 18.5 parts by weight of cyanuric chloride in 500 parts by weight of cold water. The temperature is maintained at 10 to 15 hours for 4 hours.
The hydrochloric acid formed during the condensation is neutralized by the appropriate amount of sodium carbonate. Afterwards 37;
6 parts by weight of Jes Pro products, which is obtained by reducing the acylation product from meta-nitrobenzoyl chloride and 4-amino-4'-ogy-1,1'-azo-benzene, 3'-carboxylic acid in 50.0 parts by weight of warm water dissolved, given to the monoconduction product. The temperature is increased to 40.
After 24 hours, 18 parts by weight of aniline are added and the temperature is maintained at 80 for the same time. The tertiary condensation product is formed after this time. It is deposited with sodium chloride and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH220650T | 1940-07-09 | ||
CH217241T | 1940-07-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH220650A true CH220650A (en) | 1942-04-15 |
Family
ID=25725993
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH220650D CH220650A (en) | 1940-07-09 | 1940-07-09 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH220650A (en) |
-
1940
- 1940-07-09 CH CH220650D patent/CH220650A/en unknown
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