CH201861A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH201861A CH201861A CH201861DA CH201861A CH 201861 A CH201861 A CH 201861A CH 201861D A CH201861D A CH 201861DA CH 201861 A CH201861 A CH 201861A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- dye
- bromo
- nitro
- 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-Methyl-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 1-Amino-4-nitro- 6-brom-2-benzylsulfosäure diazotiert und die Diazoverbindung mit p-Acetaminodiphenyl- amin-o-sulfosäure kuppelt.
<I>Beispiel:</I> 333 Teile des Natriumsalzes der 1-Amino- 4-nitro-6-brom-2-benzylsulfosäure werden in üblicher Weise diazotiert und die fertige Di- azolösung wird langsam zu einer Lösung von <B>328</B> Teilen des Natriumsalzes der p-Acet- aminodiphenylamin - o - sulfosäure gegeben.
Nach beendeter Kupplung wird die Lösung des Farbstoffes mit Natronlauge neutrali siert und bei etwa 40 bis 50 im Vakuum getrocknet. Der erhaltene Farbstoff zeichnet sich durch grosse Löslichkeit, schöne braune Nuancen und gute Echtheitseigenschaften aus.
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-methyl-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 been found, an azo dye with very similar properties is obtained if 1-amino-4-nitro-6-bromo-2-benzylsulfonic acid is diazotized and the diazo compound is coupled with p-acetaminodiphenylamine-o-sulfonic acid.
<I> Example: </I> 333 parts of the sodium salt of 1-amino-4-nitro-6-bromo-2-benzylsulphonic acid are diazotized in the usual way and the finished diazole solution slowly becomes a solution of 328 </B> Parts of the sodium salt of p-acetaminodiphenylamine - o - sulfonic acid are given.
After the coupling has ended, the solution of the dye is neutralized with sodium hydroxide solution and dried at about 40 to 50 in vacuo. The dye obtained is characterized by high solubility, beautiful brown nuances and good fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE201861X | 1936-08-26 | ||
CH198711T | 1938-07-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH201861A true CH201861A (en) | 1938-12-15 |
Family
ID=25723126
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH201861D CH201861A (en) | 1936-08-26 | 1937-05-14 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH201861A (en) |
-
1937
- 1937-05-14 CH CH201861D patent/CH201861A/en unknown
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