CH190720A - 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
- CH190720A CH190720A CH190720DA CH190720A CH 190720 A CH190720 A CH 190720A CH 190720D A CH190720D A CH 190720DA CH 190720 A CH190720 A CH 190720A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- new derivative
- orange
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo dyes
- C09B31/06—Disazo dyes from a coupling component "C" containing a directive hydroxyl group
- C09B31/062—Phenols
-
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Derivates eines Azofarbstoffes. Es wurde gefunden, dass man ein neues Derivat eines Azofarb@stoffes erhält, wenn man auf den Disazofarbstoff aus diazotier- tem 4'-Amino-2.3'-dimethylazobenzol und p-Kresol Chlorsulfonsäure in Gegenwart eines tertiären Base einwirken lässt.
Mas neue Produkt bildet ein orange ge färbtes Pulver, das sich in Nasser mit orangeroter Farbe löst, und durch Zugabe. von Säuren das Ausgangspigment wieder leicht regeneriert. <I>Beispiel:</I> In 1.50 Teile trockenes Pyridin trägt man unter Rühren und Kühlen mit Eis- Kochsalz 10 Teile Chlorsulfonsäure vorsich tig ein, und lässt hierauf das Reaktions- gE>miseh sich auf etwa 20 erwärmen.
Hier zu gibt man 6.8-Teile des Pigmentes aus diazotiertem 4-Amino-3.2'-dimethylazoben- zol und p-Kresol zu und erwärmt allmählich auf 60 bis<B>70',</B> und hält 3 bis 4 Stunden bei dieser Temperatur, wobei das Pigment sich allmählich auflöst, und eine klare inten siv .gelbbraun gefärbte Reaktionslösung ent steht.
Nun lässt man die Reaktionsmasse ab- ]fühlen, und giesst sie @dann in eine Lösung von 55 Teilen Natriumkarbonat in 220 Tei len Wasser. Durch Destillation mit Wasser dampf treibt man da:s Pyridin ab, kühlt den wässerigen Destillationsrückstand, und fil triert das ausgefallene feste Reaktionspro dukt ab.
Zur Entfernung von noch etwas unverändertem Ausgangsspi,gment ,löst man das Salz des erhaltenen Schwefelsäureesters in Wasser, filtriert, fällt mit Kochsalz heiss aus und putscht . ab. Das Produkt wird zweckmässig als schwach alkalisch gestellte Paste aufbewahrt.
Process for the preparation of a new derivative of an azo dye. It has been found that a new derivative of an azo dye is obtained if chlorosulfonic acid is allowed to act on the disazo dye made from diazotized 4'-amino-2,3'-dimethylazobenzene and p-cresol in the presence of a tertiary base.
Ma's new product forms an orange colored powder that dissolves in water with an orange-red color, and when added. The original pigment is easily regenerated by acids. <I> Example: </I> 10 parts of chlorosulfonic acid are carefully added to 1.50 parts of dry pyridine while stirring and cooling with ice-table salt, and the reaction is then allowed to warm to about 20.
6.8 parts of the pigment from diazotized 4-amino-3.2'-dimethylazobenzene and p-cresol are added here and the mixture is gradually heated to 60 to 70 'and held for 3 to 4 hours Temperature at which the pigment gradually dissolves and a clear, intense yellow-brown reaction solution is created.
Now you can feel the reaction mass, and then pour it into a solution of 55 parts of sodium carbonate in 220 parts of water. The pyridine is driven off by distillation with steam, the aqueous distillation residue is cooled and the precipitated solid reaction product is filtered off.
To remove the somewhat unchanged starting particle, the salt of the sulfuric acid ester obtained is dissolved in water, filtered, precipitated while hot with common salt and putted. from. The product is conveniently stored as a slightly alkaline paste.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH190720T | 1936-04-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH190720A true CH190720A (en) | 1937-05-15 |
Family
ID=4437176
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH190720D CH190720A (en) | 1936-04-09 | 1936-04-09 | Process for the preparation of a new derivative of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH190720A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3045004A (en) * | 1959-04-16 | 1962-07-17 | Acna | Disazo dyes |
-
1936
- 1936-04-09 CH CH190720D patent/CH190720A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3045004A (en) * | 1959-04-16 | 1962-07-17 | Acna | Disazo dyes |
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