CH151168A - Process for the preparation of a wool dye. - Google Patents
Process for the preparation of a wool dye.Info
- Publication number
- CH151168A CH151168A CH151168DA CH151168A CH 151168 A CH151168 A CH 151168A CH 151168D A CH151168D A CH 151168DA CH 151168 A CH151168 A CH 151168A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- wool
- parts
- dye
- wool dye
- 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 1Vlol. 4'-tlthoxy-2. 6-diaminodiphenyl- amin-4-sulfosäure mit 11VIol. 2.4.6-Trinitro- alkoxybenzo1 kondensiert.
Hierbei findet zu nächst die zu erwartende Reaktion zwischen der Alkoxygruppe und einer Aminogruppe statt, bei weiterem Erhitzen in Gegenwart Yon Alkali tritt dann aber unter Abspaltung von Alkalinitrit eine innere Kondensation Ein.
<I>Beispiel:</I> 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 Wasser neutral gelöst und bei 70 bis 80 mit 24 Teilen 2. 4 .
6-Trinitroanisol, welches man allmählich unter Rühren zugibt, kon- densiert. Gleichzeitig lässt man eine Lösung von 6 Teilen Natriumkarbonat in 60 Teilen Wasser zutropfen. Nachdem alles Trinitro- anisol umgesetzt ist, gibt man noch 6 Teile Natriumkarbonat hinzu und erhitzt eine Stunde auf 90 . Der Farbstoff wird durch Aussalzen abgeschieden und getrocknet. 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 lightfastness, if one 1 vol. 4'-thoxy-2. 6-diaminodiphenylamine-4-sulfonic acid with 11VIol. 2.4.6-trinitroalkoxybenzo1 condensed.
In this case, the reaction to be expected between the alkoxy group and an amino group takes place first, but on further heating in the presence of alkali, an internal condensation then occurs with elimination of alkali metal nitrite.
<I> Example: </I> 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 like Reduction of the nitro groups are dissolved in 500 parts of water and neutralized at 70 to 80 with 24 parts 2. 4.
6-trinitroanisole, which is gradually added with stirring, condenses. At the same time, a solution of 6 parts of sodium carbonate in 60 parts of water is added dropwise. After all the trinitroanisole has reacted, 6 parts of sodium carbonate are added and the mixture is heated to 90 for one hour. The dye is deposited by salting out and dried. It forms a black powder.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE151168X | 1929-08-17 | ||
CH147460T | 1931-06-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH151168A true CH151168A (en) | 1931-11-30 |
Family
ID=25715036
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH151168D CH151168A (en) | 1929-08-17 | 1930-03-12 | Process for the preparation of a wool dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH151168A (en) |
-
1930
- 1930-03-12 CH CH151168D patent/CH151168A/en unknown
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