CH209559A - Process for the production of a new dye preparation. - Google Patents
Process for the production of a new dye preparation.Info
- Publication number
- CH209559A CH209559A CH209559DA CH209559A CH 209559 A CH209559 A CH 209559A CH 209559D A CH209559D A CH 209559DA CH 209559 A CH209559 A CH 209559A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- dye preparation
- new dye
- pyridine
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> 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-dimethoxy-4-aminocarbäthoxybenzol und dem Anilid der 2,3-Oxynaphthoesäure Ben- zoesäure-3-sulfochlorid 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. <I>Beispiel:</I> Man verrührt 25,7 Teile des Kupplungs produktes aus dianotiertem 1-Amino-2,5-di- methogy-4-aminocarbäthoxy-benzol und 2,3 Oxynaphthoesäureanilid mit 150 Teilen Py- ridin bei 50-550. Zum Gemenge lässt man 33 Teile geschmolzene Benzoesäure-3-sulfo- chlorid 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 Reak- tionsgemisch auf<B>500</B> abkühlen und destilliert einen Teil des Pyridins im Vakuum ab. Den Rückstand löst man in warmem Wasser, bin det das Pyridin mit Säure, z. B. wässeriger Salzsäure, und fällt das Kondensationsprodukt mit aussalzenden Mitteln, z. B. Natriumehlorid.
<B> Additional patent </B> 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 made from dianotized 1-amino-2,5-dimethoxy-4-aminocarbethoxybenzene and the anilide of 2,3-oxynaphthoic acid benzoic acid-3-sulfochloride in Let the presence of 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. <I> Example: </I> 25.7 parts of the coupling product of dianotized 1-amino-2,5-dimethogy-4-aminocarbethoxy-benzene and 2,3 oxynaphthoic anilide are stirred with 150 parts of pyridine at 50 -550. 33 parts of molten benzoic acid 3-sulfochloride are allowed to flow into the mixture while the temperature is increased,
and stir 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 <B> 500 </B> and some of the pyridine is distilled off in vacuo. The residue is dissolved in warm water, bind the pyridine with acid, z. B. aqueous hydrochloric acid, and the condensation product falls with salting-out agents, e.g. B. Sodium chloride.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH209559T | 1938-07-02 | ||
CH206722T | 1938-07-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH209559A true CH209559A (en) | 1940-04-15 |
Family
ID=25724339
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH209559D CH209559A (en) | 1938-07-02 | 1938-07-02 | Process for the production of a new dye preparation. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH209559A (en) |
-
1938
- 1938-07-02 CH CH209559D patent/CH209559A/en unknown
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