CH151164A - Process for the preparation of a wool dye. - Google Patents
Process for the preparation of a wool dye.Info
- Publication number
- CH151164A CH151164A CH151164DA CH151164A CH 151164 A CH151164 A CH 151164A CH 151164D A CH151164D A CH 151164DA CH 151164 A CH151164 A CH 151164A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- wool
- parts
- mol
- dye
- Prior art date
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- Coloring (AREA)
Description
Verfahren zur Darstellung eines Wollfarbstoffes. <B>-</B> Wie gefunden wurde, gelangt man zu einem neuen -wertvollen Farbstoff, der Wolle in braunen, gut egalisierenden Tönen von sehr guter Lielitechtheit färbt, -wenn man <B>1</B> Mol. 4'-Methyl-2. 6-dia.minodiphenyla-min- 4-sulfosäure mit<B>1</B> Mol. 2. 4. 6-Triiiitro-l- alkoxybenzol kondensiert.
Hierbei findet zu nächst die zu erwartende Reaktion zwischen der Alkox gruppe und einer Aminogruppe y tn statt, bei weiterem Erhitzen in Gegenwart von Alkali tritt dann aber unter Abspaltung von Alkalinitrit eine innere Kondensation ein, <I>Beispiel:
</I> <B>29,3</B> Teile 4-Methyl-2. 6-diaminodiphe- nylamin-4-suliosäure, erhalten durch Kon- densation von 2.<B>6 -</B> Dinitrochlorbenzol <B>-</B> 4 - sulfosäure mit p-Toluidin und folgender Re duktion der Nitrogruppen, werden in<B>500</B> Teilen Wasser neutral gelöst und bei<B>70</B> bis <B>80 '</B> mit 24 Teilen 2. 4. 6-Trinitroanisol, welches man allmählich unter Rühren zu- gibt, kondensiert.
Gleichzeitig lässt man eine Lösun" von<B>6</B> Teilen Natriumkarbonat in<B>60</B> Teilen Wasser zutropfen. Nachdem alles Trinitroanisol 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 getrock net. Er bildet ein schwarzes Pulver.
Process for the preparation of a wool dye. <B> - </B> As has been found, a new, valuable dye is obtained, which dyes wool in brown, well-leveling shades of very good Lielite fastness, -if one <B> 1 </B> Mol. 4 ' -Methyl-2. 6-dia.minodiphenyla-min-4-sulfonic acid with <B> 1 </B> Mol. 2. 4. 6-Triiiitro-1-alkoxybenzene condensed.
In this case, the reaction to be expected between the alkoxy group and an amino group y tn takes place first, but with further heating in the presence of alkali, an internal condensation then occurs with elimination of alkali metal nitrite, <I> Example:
</I> <B> 29.3 </B> parts 4-methyl-2. 6-diaminodiphenylamine-4-sulio acid, obtained by condensation of 2. 6 - </B> dinitrochlorobenzene <B> - </B> 4 - sulphonic acid with p-toluidine and subsequent reduction of the nitro groups, are dissolved neutrally in <B> 500 </B> parts of water and at <B> 70 </B> to <B> 80 '</B> with 24 parts 2. 4. 6-trinitroanisole, which is gradually added with stirring admits, condenses.
At the same time, a solution of <B> 6 </B> parts of sodium carbonate in <B> 60 </B> parts of water is added dropwise. After all of the trinitroanisole has reacted, <B> 6 </B> parts of sodium carbonate are added and heated to <B> 90 'for one hour. </B> The dye is deposited by salting out and dried, forming a black powder.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE151164X | 1929-08-17 | ||
CH147460T | 1931-06-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH151164A true CH151164A (en) | 1931-11-30 |
Family
ID=25715032
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH151164D CH151164A (en) | 1929-08-17 | 1930-03-12 | Process for the preparation of a wool dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH151164A (en) |
-
1930
- 1930-03-12 CH CH151164D patent/CH151164A/en unknown
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