CH151160A - Process for the preparation of a wool dye. - Google Patents
Process for the preparation of a wool dye.Info
- Publication number
- CH151160A CH151160A CH151160DA CH151160A CH 151160 A CH151160 A CH 151160A CH 151160D A CH151160D A CH 151160DA CH 151160 A CH151160 A CH 151160A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- dye
- parts
- wool
- hol
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfalwen zur Darstellung elues WoRfarbstoffes. Wie gefunden wurde, gelangt man zu einem neuen wertvollen Farbstoff, der Wolle in gelbbraunen, gut egalisierenden Tönen von sehr guter Lielitechtlieit färbt, wenn man<B>1</B> Hol. 2.6-Diaminodiplienylamin-4- suliosäure mit<B>1</B> Hol. 2. 4. 6-Trinitro-l- alkoxybenzol kondensiert.
Hierbei findet zu nächst die zu erwarten-de Reaktion zwischen der Alkoxygruppe und einer Aminogruppe statt, bei weiterem Erhitzen in Gegen-wart -von Alkali tritt dann aber unter Abspaltung von Alkalinitrit eine innere Kondensation ein.
<I>Beispiel:</I> <B>27,9</B> Teile<B>*</B> 2. 6-Diaminodiphenylamin-4- sulfosäure, erhalten durch Kondensation von 2.<B>6 -</B> Dinitrochlorbenzol <B>-</B> 4<B>-</B> sulfosäure mit Anilin und folgende Reduktion der Nitro- gruppen, werden in<B>500</B> Teilen Wasser neu tral gelöst und bei<B>70</B> bis<B>80 '</B> mit 24 Teilen 2. 4. 6-'Prinitroaniso.1, welches man allmäh- lieh unter Rühren zugibt, kondensiert.
Gleichzeitig lässt man eine Lösung von <B>6</B> Teilen Natriumkarbonat in<B>60</B> Teilen Wasser zutropfen. Nachdem alles Trinitro- anisol umgesetzt ist, gibt man noch<B>6</B> Teile Natriumkarbonat hinzu und erhitzt eine Stunde auf<B>90</B> '. Der Farbstoff wird durch Aussalzen abgeschieden und stellt getrock net ein schwarzes Pulver dar.
Procedure for the representation of the eluent dye. As has been found, one arrives at a new valuable dye which dyes wool in yellow-brown, well-leveling shades of very good lightfastness if one <B> 1 </B> takes it. 2,6-diaminodiplienylamine-4-sulio acid with <B> 1 </B> hol. 2. 4. 6-trinitro-1-alkoxybenzene condensed.
In this case, the reaction to be expected between the alkoxy group and an amino group initially takes place, but if the alkali is heated further in the presence of alkali, an internal condensation then occurs with the elimination of alkali metal nitrite.
<I> Example: </I> <B> 27.9 </B> parts <B> * </B> 2. 6-diaminodiphenylamine-4-sulfonic acid, obtained by condensation of 2. <B> 6 - < / B> Dinitrochlorobenzene <B> - </B> 4 <B> - </B> sulfonic acid with aniline and subsequent reduction of the nitro groups are neutralized in <B> 500 </B> parts of water and < B> 70 </B> to <B> 80 '</B> with 24 parts 2. 4. 6-'Prinitroaniso.1, which is gradually added with stirring, condensed.
At the same time, a solution of 6 parts of sodium carbonate in 60 parts of water is added dropwise. After all of the trinitroanisole has been converted, <B> 6 </B> parts of sodium carbonate are added and the mixture is heated to <B> 90 </B> 'for one hour. The dye is deposited by salting out and is a black powder when dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE151160X | 1929-08-17 | ||
CH147460T | 1931-06-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH151160A true CH151160A (en) | 1931-11-30 |
Family
ID=25715028
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH151160D CH151160A (en) | 1929-08-17 | 1930-03-12 | Process for the preparation of a wool dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH151160A (en) |
-
1930
- 1930-03-12 CH CH151160D patent/CH151160A/en unknown
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