CH170926A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH170926A CH170926A CH170926DA CH170926A CH 170926 A CH170926 A CH 170926A CH 170926D A CH170926D A CH 170926DA CH 170926 A CH170926 A CH 170926A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- dye
- blue
- dinitro
- Prior art date
Links
Landscapes
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Azofarbstoffes. Nach dem im Hauptpatent beschriebenen Verfahren erhält man einen blauen Acetat seidenfarbstoff, wenn man dianotiertes 6-Broin- 2.4-dinitro-l-aminoberizol mit 1-Aininonaph- thalin kuppelt.
Wie nun weiter gefunden wurde, erhält man einen Farbstoff mit ganz ähnlichen Eigenschaften, wenn man 6-Broin-2.4-dinitro- 1-aminobenzol dianotiert und mit 1-'Methyl- 3-oxyäthylbutylaminobenzol kuppelt.
<I>Beispiel</I> 29 Teile 6-Brom-2.4-dinitro-l-aminobenzol werden dianotiert, indem man die Verbindung bei einer Temperatur vor) etwa<B>55</B> in eine mit 6,9 Teilen Natriumnitrit und 120 Teilen konzentrierter Schwefelsäure bereitete Nitro- syIschwefelsäure einrührt. Durch Digerieren in der mehrfachen Menge Eis wird eine sehr leicht kuppelnde Diazolösung erhalten, die man nach dem Filtrieren in eine schwach mineralsaure Lösung von 20,7 Teilen 1-Me- thyl-3-oxyäthyl-butylaminoberizol einlaufen lässt. Die Kupplung vollzieht sich rasch, auch ohne Zusatz eines säurebindenden Mittels.
Der fertige Farbstoff erzeugt auf Acetatseide ein Blauviolett von vorzüglicher Lichtechtheit.
Process for the preparation of an azo dye. According to the process described in the main patent, a blue acetate silk dye is obtained when dianotated 6-broin-2,4-dinitro-1-aminoberizole is coupled with 1-ainonaphthalene.
As has now been further found, a dye with very similar properties is obtained if 6-broin-2,4-dinitro-1-aminobenzene is dianotized and coupled with 1-methyl-3-oxyethylbutylaminobenzene.
<I> Example </I> 29 parts of 6-bromo-2,4-dinitro-1-aminobenzene are dianotized by adding the compound at a temperature of about 55 to 6.9 parts of sodium nitrite and 120 parts of concentrated sulfuric acid is stirred in nitro-sysulfuric acid. Digestion in a multiple amount of ice gives a very easily coupling diazo solution which, after filtering, is allowed to run into a weakly mineral acidic solution of 20.7 parts of 1-methyl-3-oxyethyl-butylaminoberizole. The coupling takes place quickly, even without the addition of an acid-binding agent.
The finished dye produces a blue-violet of excellent lightfastness on acetate silk.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE170926X | 1932-07-08 | ||
CH168144T | 1933-04-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH170926A true CH170926A (en) | 1934-07-31 |
Family
ID=25718526
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH170926D CH170926A (en) | 1932-07-08 | 1933-04-27 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH170926A (en) |
-
1933
- 1933-04-27 CH CH170926D patent/CH170926A/en unknown
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