CH217242A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH217242A CH217242A CH217242DA CH217242A CH 217242 A CH217242 A CH 217242A CH 217242D A CH217242D A CH 217242DA CH 217242 A CH217242 A CH 217242A
- Authority
- CH
- Switzerland
- Prior art keywords
- sulfonic acid
- preparation
- methyl
- dye
- benzothiazole
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/0025—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Dlonoazofarbstoffes. Es wurde gefunden, dass man wertvolle Monoazofarbstoffe erhält, wenn man die Di- azoverbindungen aus Aminen von der all gemeinen Formel:
EMI0001.0004
mit Acetoacetylverbindungen von der allgemeinen Formel:
EMI0001.0007
worin X für Wasserstoff oder eine Sulfon- säuregruppe, Y für Methyl oder eine Carb- oxylgruppe und Z für Wasserstoff oder eine .1, stehen, kuppelt und die erhal- 31 tenen Farbstoffe gegebenenfalls sulfoniert, wobei der fertige Farbstoff mindestens 2 Sul- fonsäuregruppen enthalten soll.
Gegenstand des vorliegenden Patentes ist ein Verfahren zur Herstellung eines Mono azofarbstoffes, welches dadurch gekennzeich- net ist, daB man die Diazoverbindung der ?-(4' - Aminopheny l)-6-methyl-benzothiazol- 7 - sulfonsäure mit 2 - (4' - Acetoacetylamino- phenyl)-6-methyl-benzothiazol- 7-sulfonsäure kuppelt.
Der neue Azofarbstoff stellt ein gelles Pulver dar und zieht gut auf Baumwolle und Viskose.
Beispiel: <B>320</B> Gewichtsteile 2-(4'- Aminopheny 1)-6 methylbenzothiazol-7-sulfonsäurewerden wie üblich diazotiert. Die Suspension der Diazo- verbindung wird dann in eine Lösung von 404 Gewichtsteilen 2-(4'-Acetoacetylamino- phenyl)-6-methylbenzothiazol- 7 -sulfonsäure (erhältlich durch Einwirkung von Diketen auf ?-(4'- Aminophenyl)-6-methylben7othi- azol-7-sulfonsäure)
und 212 Gewichtsteilen Natriumearbonat in Wasser eingetragen. Nach beendeter Kupplung wird der Farb- loff ausgesalzen, abgesaugt und getrocknet. Er stellt ein gelle: Pulver dar. das sehn gut auf Baumwolle und Viskose zieht. Die er haltenen grünstichig gelben Färbungen zeich nen sich durch sehr gute Wasser- und Waschechtheit und gute Lichtechtheit aus.
Auf einem Mischgewebe aus 50 Teilen Baumwolle und 50 Teilen Zellwolle aus Vis kose erhält man eine grünstichig gelbe Ton- in-Ton-Färbung.
Process for the preparation of a dlonoazo dye. It has been found that valuable monoazo dyes are obtained if the diazo compounds from amines have the general formula:
EMI0001.0004
with acetoacetyl compounds of the general formula:
EMI0001.0007
where X is hydrogen or a sulfonic acid group, Y is methyl or a carboxyl group and Z is hydrogen or a .1, couples and sulfonates the resulting dyes, if necessary, the finished dye containing at least 2 sulfonic acid groups should.
The subject of the present patent is a process for the production of a mono azo dye, which is characterized in that the diazo compound of? - (4 '- aminophenyl) -6-methyl-benzothiazole- 7-sulfonic acid is mixed with 2 - (4' - Acetoacetylaminophenyl) -6-methyl-benzothiazole- 7-sulfonic acid couples.
The new azo dye is a yellow powder and absorbs well on cotton and viscose.
Example: <B> 320 </B> parts by weight of 2- (4'-aminopheny 1) -6 methylbenzothiazole-7-sulfonic acid are diazotized as usual. The suspension of the diazo compound is then dissolved in a solution of 404 parts by weight of 2- (4'-acetoacetylaminophenyl) -6-methylbenzothiazole-7-sulfonic acid (obtainable by the action of diketene on? - (4'-aminophenyl) -6- methylben7othiazole-7-sulfonic acid)
and 212 parts by weight of sodium carbonate added to water. After the coupling is complete, the dye is salted out, filtered off with suction and dried. It represents a bright: powder. It looks good on cotton and viscose. The greenish yellow dyeings obtained are distinguished by very good water and wash fastness and good light fastness.
A greenish yellow tone-on-tone coloration is obtained on a mixed fabric of 50 parts of cotton and 50 parts of viscose rayon.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE217242X | 1939-11-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH217242A true CH217242A (en) | 1941-10-15 |
Family
ID=5830647
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH217242D CH217242A (en) | 1939-11-07 | 1940-09-19 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH217242A (en) |
-
1940
- 1940-09-19 CH CH217242D patent/CH217242A/en unknown
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