CH151167A - Process for the preparation of a wool dye. - Google Patents
Process for the preparation of a wool dye.Info
- Publication number
- CH151167A CH151167A CH151167DA CH151167A CH 151167 A CH151167 A CH 151167A CH 151167D A CH151167D A CH 151167DA CH 151167 A CH151167 A CH 151167A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- wool
- parts
- dye
- sulfonic acid
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Wollfarbstoffes. Wie gefunden wurde, gelangt man zu, einem neuen wertvollen Farbstoff, der Wolle in rötlichbraunen, gut egalisierenden Tönen von sehr guter Lichtechtheit färbt, wenn man 1 hIol. 4' Athoxy-2 .
6-diaminodiphenyl- amin-4-sulfosäure mit 1 Mol. 2.4.6-Tri- nitro-l-chlorbenzol kondensiert. Hierbei fin det zunächst die zu erwartende Reaktion zwi schen dem Chloratom und einer Amino- Kruppe statt, bei weiterem Erhitzen in Geo-enwart von Alkali tritt dann aber unter Abspaltung von Alkalinitrit eine innere Kon densation ein.
Beispiel: 32,3 Teile 4'-Äthoxy-2.6-diaminodiphe- nylamin-4-sulfosäure, erhalten durch Kon densation von 2. 6-Dinitrochlorbenzol-4-sulfo- säure mit p-Phenetidin und folgende Reduk tion der Nitrogruppen, werden in 500 Teilen 1ATasser neutral gelöst und bei 70 bis 80 mit 24 Teilen 2.4.6-Trinitrochlorbenzol, welches man allmählich unter Rühren zu- gibt, kondensiert.
Gleichzeitig lässt man eine Lösung von 11 Teilen Natriumkarbonat in 110 Teilen Wasser zutropfen. Nachdem alles Trinitrochlorbenzol umgesetzt ist, gibt man noch 6 Teile Natriumkarbonat hinzu und er hitzt eine Stunde auf<B>90'.</B> Der Farbstoff wird durch Aussalzen abgeschieden und ge trocknet. Er bildet ein schwarzes Pulver.
Process for the preparation of a wool dye. As has been found, one arrives at a new valuable dye which dyes wool in reddish-brown, well-leveling shades of very good fastness to light, if one hIol. 4 'athoxy-2.
6-diaminodiphenylamine-4-sulfonic acid condensed with 1 mol. 2.4.6-tri-nitro-1-chlorobenzene. In this case, the expected reaction between the chlorine atom and an amino group takes place first, but with further heating in the presence of alkali, internal condensation then occurs with the elimination of alkali metal nitrite.
Example: 32.3 parts of 4'-ethoxy-2,6-diaminodiphenylamine-4-sulfonic acid, obtained by condensation of 2. 6-dinitrochlorobenzene-4-sulfonic acid with p-phenetidine and the following reduction of the nitro groups, are in 500 parts of 1A water dissolved in a neutral state and condensed at 70 to 80 with 24 parts of 2,4,6-trinitrochlorobenzene, which is gradually added with stirring.
At the same time, a solution of 11 parts of sodium carbonate in 110 parts of water is added dropwise. After all of the trinitrochlorobenzene has reacted, 6 parts of sodium carbonate are added and it is heated to <B> 90 'for one hour. </B> The dye is separated out by salting out and dried. It forms a black powder.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE151167X | 1929-08-17 | ||
CH147460T | 1931-06-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH151167A true CH151167A (en) | 1931-11-30 |
Family
ID=25715035
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH151167D CH151167A (en) | 1929-08-17 | 1930-03-12 | Process for the preparation of a wool dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH151167A (en) |
-
1930
- 1930-03-12 CH CH151167D patent/CH151167A/en unknown
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