CH140328A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH140328A CH140328A CH140328DA CH140328A CH 140328 A CH140328 A CH 140328A CH 140328D A CH140328D A CH 140328DA CH 140328 A CH140328 A CH 140328A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- dye
- methyl
- pyrazolone
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Im Hauptpatent ist ein Verfahren zur Herstellung eines Azofarbstoffes beschrieben, bei dem man die Diazoverbindung des An- thranilsäure-n-butylesters mit 1-(4'-Sulfophe- nyl)-3-methyl-5-pyrazolon kombiniert.
Es wurde nun gefunden, dass man eben falls einen wertvollen Azofarbstoff erhält, wenn man die Diazoverbindung des Anthra- nilsäure-n-butylesters mit 1-(5'-Sulfo-2'-chlor- phenyl)-3-methyl-5-pyrazolon kombiniert. Der erhaltene Farbstoff färbt Wolle in grünstichig gelben, sehr echten Tönen.
<I>Beispiel:</I> Die wässerige Lösung der in der üblichen Weise erhaltenen Diazoverbindungen von 29,1 Teilen Anthrariilsäure-n-butylestersulfat lässt man in eine wässerige Lösung von 29,0 Tei len 1-(5'-Sulfo-2'-chlorphenyl)-3-methyl-5-py- razolon und 150 Teilen wasserfreier Soda einfliessen. Nach etwa 2-3 Stunden langem Rühren wird der entstandene Farbstoff ab gesaugt.
Process for the preparation of an azo dye. The main patent describes a process for the preparation of an azo dye in which the diazo compound of n-butyl anthranilate is combined with 1- (4'-sulfophenyl) -3-methyl-5-pyrazolone.
It has now been found that a valuable azo dye is also obtained if the diazo compound of n-butyl anthranolate is obtained with 1- (5'-sulfo-2'-chlorophenyl) -3-methyl-5-pyrazolone combined. The dye obtained dyes wool in greenish yellow, very real shades.
<I> Example: </I> The aqueous solution of the diazo compounds obtained in the usual way of 29.1 parts of anthrariic acid n-butyl ester sulfate is allowed to pour into an aqueous solution of 29.0 parts of 1- (5'-sulfo-2 '-chlorophenyl) -3-methyl-5-py- razolon and 150 parts of anhydrous soda flow in. After stirring for about 2-3 hours, the resulting dye is sucked off.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE140328X | 1927-11-17 | ||
CH138601T | 1928-10-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH140328A true CH140328A (en) | 1930-05-31 |
Family
ID=25713220
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH140328D CH140328A (en) | 1927-11-17 | 1928-10-10 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH140328A (en) |
-
1928
- 1928-10-10 CH CH140328D patent/CH140328A/en unknown
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