CH201860A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH201860A CH201860A CH201860DA CH201860A CH 201860 A CH201860 A CH 201860A CH 201860D A CH201860D A CH 201860DA CH 201860 A CH201860 A CH 201860A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- dye
- diazotized
- sulfonic acid
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Gemäss dem im Hauptpatent beschrie benen Verfahren erhält man einen Leder in braunen Tönen färbenden Azofarbstoff, wenn man 2-3Zethyl-6-brom-4-nitro-l-aminobenzol diazotiert und die Diazoverbindung mit Di- phenylamin-2-carbon-2'-sulfosäure kuppelt.
Wie nun weiter gefunden wurde, erhält man einen Azofarbstoff von ganz ähnlichen Eigenschaften, wenn man 2-Methyl-6-chlor- 4-nitranilin diazotiert und die Diazoverbin- dung mit p-Acetaminodiphenylamin-o-sulfo- säure kuppelt.
<I>Beispiel:</I> 186,5 Teile 2-Methyl-6-chlor-4-nitranilin werden in üblicher Weise mittels Nitrosyl- sehwefelsäure diazotiert. Die wässerige Di- azolösung wird nicht zu rasch zu einer Lö sung von 328 Teilen des Natriumsalzes der p-Acetaminodiphenylamin-o-sulfosäure gege- ben. Nach längerem Rühren wird der Farb stoff ausgesalzen, filtriert, gewaschen,
in das Natriumsalz übergeführt und getrocknet. Er ist ein dunkles Pulver, welches Leder in braunen Tönen von sehr guten Echtheits eigenschaften färbt.
Process for the preparation of an azo dye. According to the process described in the main patent, an azo dye which dyes leather in brown shades is obtained if 2-3zethyl-6-bromo-4-nitro-1-aminobenzene is diazotized and the diazo compound is treated with diphenylamine-2-carbon-2'- sulfonic acid couples.
As has now also been found, an azo dye with very similar properties is obtained if 2-methyl-6-chloro-4-nitroaniline is diazotized and the diazo compound is coupled with p-acetaminodiphenylamine-o-sulfonic acid.
<I> Example: </I> 186.5 parts of 2-methyl-6-chloro-4-nitroaniline are diazotized in the customary manner using nitrosylsulfuric acid. The aqueous diazole solution is not added too quickly to a solution of 328 parts of the sodium salt of p-acetaminodiphenylamine-o-sulfonic acid. After prolonged stirring, the dye is salted out, filtered, washed,
converted into the sodium salt and dried. It is a dark powder which dyes leather in brown tones with very good fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE201860X | 1936-08-26 | ||
CH198711T | 1938-07-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH201860A true CH201860A (en) | 1938-12-15 |
Family
ID=25723125
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH201860D CH201860A (en) | 1936-08-26 | 1937-05-14 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH201860A (en) |
-
1937
- 1937-05-14 CH CH201860D patent/CH201860A/en unknown
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