CH209558A - Process for the production of a new dye preparation. - Google Patents
Process for the production of a new dye preparation.Info
- Publication number
- CH209558A CH209558A CH209558DA CH209558A CH 209558 A CH209558 A CH 209558A CH 209558D A CH209558D A CH 209558DA CH 209558 A CH209558 A CH 209558A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- dye preparation
- new dye
- dye
- 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
- C09B43/124—Preparation of azo dyes from other azo compounds by acylation of amino groups with monocarboxylic acids, carbamic esters or halides, mono- isocyanates, or haloformic acid esters
-
- 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
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
Description
Zusatzpatent zum Hauptpatent Nr. 206722. Verfahren zur Herstellung eines neuen Farbstoffpräparates. Es wurde gefunden, dass man ein neues, lösliches Farbstoffpräparat erhält, wenn man auf den Azofarbstoff aus dianotiertem 1-Amino- 2,5-diäthoxy-4-aminocarbäthoxybenzol und dem o-Toluidid der 2.3-Oxynaphthoesäure Benzoylchlorid-m-sulfosäure in Gegenwart von Pyridin einwirken lässt.
Das neue Präparat bildet ein dunkel gefärbtes Pulver, das sich in Wasser mit brauner Farbe löst und auf Zusatz von Alkalien den Ausgangsfarbstoff wieder abscheidet. Es kann zum Färben oder Drucken von Textilien verwendet werden. Beispiel Man verrührt 27,8 Teile des Kupplungs produktes aus dianotiertem 1-Amino-2,5-di- äthoxy-4-aminocarbäthoxy-benzol und 2,3- Oxynaphthoesäure-o-toluidid mit 150 Teilen Pyridin bei 50-55 .
Zum Gemenge lässt man 33 Teile geschmolzene Benzoylchlorid-m-sulfo- säure unter Steigenlassen der Temperatur zufliessen, und rührt noch einige Zeit bei 110-115 . Sobald eine klare, braune Lösung entstanden und eine Probe in Wasser klar löslich geworden ist, lässt man das Reaktions- gemisch auf 50<B>'</B>abkühlen und destilliert einen Teil des Pyridins im Vakuum ab. Den Rück stand löst man in warmem Wasser, bindet das Pyridin mit Säure, z. B. wässeriger Salz säure, und fällt das Kondensationsprodukt mit aassalzenden Mitteln, z. B. Natrium chlorid.
Additional patent to main patent No. 206722. Process for the production of a new dye preparation. It has been found that a new, soluble dye preparation is obtained if the azo dye of dianotized 1-amino-2,5-diethoxy-4-aminocarbethoxybenzene and the o-toluidide of 2,3-oxynaphthoic acid is benzoyl chloride-m-sulfonic acid in the presence of Lets pyridine act.
The new preparation forms a dark colored powder that dissolves in water with a brown color and, when alkalis are added, redeposits the original pigment. It can be used for dyeing or printing textiles. EXAMPLE 27.8 parts of the coupling product of dianotized 1-amino-2,5-diethoxy-4-aminocarbethoxy-benzene and 2,3-oxynaphthoic acid-o-toluidide are stirred with 150 parts of pyridine at 50-55.
33 parts of molten benzoyl chloride-m-sulfonic acid are allowed to flow into the mixture, while the temperature is increased, and the mixture is stirred for some time at 110-115. As soon as a clear, brown solution has formed and a sample has become clearly soluble in water, the reaction mixture is allowed to cool to 50 and some of the pyridine is distilled off in vacuo. The residue was dissolved in warm water, the pyridine binds with acid, z. B. aqueous hydrochloric acid, and the condensation product falls with aassalzenden agents, for. B. sodium chloride.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH206722T | 1938-07-02 | ||
CH209558T | 1938-07-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH209558A true CH209558A (en) | 1940-04-15 |
Family
ID=25724338
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH209558D CH209558A (en) | 1938-07-02 | 1938-07-02 | Process for the production of a new dye preparation. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH209558A (en) |
-
1938
- 1938-07-02 CH CH209558D patent/CH209558A/en unknown
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