CH189052A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH189052A CH189052A CH189052DA CH189052A CH 189052 A CH189052 A CH 189052A CH 189052D A CH189052D A CH 189052DA CH 189052 A CH189052 A CH 189052A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- monoazo dye
- pyrazolone
- phenyl
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Dionoazofarbstoffes. Gemäss dem im Hauptpatent beschriebenen Verfahren erhält man einen Wolle in echten Tönen anfärbenden Azofarbstoff, wenn man Anthranilsäure dianotiert und die Diazover- bindung mit einem Pyrazolon kuppelt, wel ches in der 1-Stellung durch einen Phenylrest substituiert ist, der noch durch einen Sulfo- amidophenylrest weiter substituiert ist.
Wie nun weiter gefunden wurde, erhält man einen Farbstoff von ganz ähnlichen Eigenschaften, wenn man 4-Nitro-6-chlor-2- amino-l-oxybeiizol dianotiert und die Diazo- verbindung mit 1-(Phenyl-4'-carbonsäure- anilid - 3"- sulfosäure) - 3 - methyl- "5 -pyrazolon kombiniert. <I>Beispiel:</I> 37 Teile 1-(Phenyl-4'-carbonsäureanilid-3"- sulfosäure)-3-methyl-5-pyrazolon werden in Wasser mit Soda gelöst.
Zu der mit über schüssiger Soda versetzten Lösung gibt man eine aus 18,9 Teilen 4-Nitro-6-chlor-2-amino- 1-oxybenzol hergestellte Diazoverbindung. Nach Beendigung der Farbstoffbildung wird erwärmt, ausgesalzen und abgesaugt. Der getrocknete Farbstoff löst sich leicht in Wasser und färbt Wolle nach dem Einbadchromver- fahren in orange Tönen von guten Echtheits eigenschaften an.
Process for the preparation of a dionoazo dye. According to the process described in the main patent, an azo dye which dyes wool in real shades is obtained if anthranilic acid is dianotized and the diazo compound is coupled with a pyrazolone which is substituted in the 1-position by a phenyl radical which is also substituted by a sulfoamidophenyl radical is further substituted.
As has now been further found, a dye with very similar properties is obtained if 4-nitro-6-chloro-2-amino-1-oxybeiizole is dianotized and the diazo compound with 1- (phenyl-4'-carboxylic acid anilide - 3 "- sulfonic acid) - 3 - methyl-" 5 -pyrazolone combined. <I> Example: </I> 37 parts of 1- (phenyl-4'-carboxylic acid anilide-3 "-sulfonic acid) -3-methyl-5-pyrazolone are dissolved in water with soda.
A diazo compound prepared from 18.9 parts of 4-nitro-6-chloro-2-amino-1-oxybenzene is added to the solution with excess soda. After the dye formation has ended, it is heated, salted out and suction filtered. The dried dye dissolves easily in water and dyes wool in orange shades with good fastness properties using the single-bath chrome process.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE189052X | 1934-06-29 | ||
CH185147T | 1935-05-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH189052A true CH189052A (en) | 1937-01-31 |
Family
ID=25721168
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH189052D CH189052A (en) | 1934-06-29 | 1935-05-29 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH189052A (en) |
-
1935
- 1935-05-29 CH CH189052D patent/CH189052A/en unknown
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