CH151162A - Process for the preparation of a wool dye. - Google Patents
Process for the preparation of a wool dye.Info
- Publication number
- CH151162A CH151162A CH151162DA CH151162A CH 151162 A CH151162 A CH 151162A CH 151162D A CH151162D A CH 151162DA CH 151162 A CH151162 A CH 151162A
- 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 braunen, gut egalisierenden Tönen von sehr guter Lichtechtheit färbt, wenn man 1 Mol. 3'-Methyl-2.6-diaminodiphenylamin- 4-sulfosäure mit 1 Mol. 2.4.6-Trinitro-l- alkoxybenzol kondensiert.
Hierbei findet zu nächst die zu erwartende Reaktion zwischen der Alkoxygruppe und einer Aminogruppe statt, bei weiterem Erhitzen in Gegenwart von Alkali tritt dann aber unter Abspaltung von Alkalinitrit eine innere Kondensation ein.
<I>Beispiel:</I> 29;3 Teile 3'-Methyl-2.6-diaminodiphe- nylamin-4-sulfosäure, erhalten durch gon. densation von 2. 6 - Dinitrochlorbenzol - 4 - sulfosäure mit m-Toluidin und folgender Re duktion der 1\Titrogruppen, werden in 500 Teilen Wasser neutral .gelöst und bei 70 bis 80 mit 24 Teilen 2. 4 . 6-Trinitroanisol, welches man allmählich unter Rühren zu- gibt, kondensiert.
Gleichzeitig lässt man eine Lösung von 6 Teilen Natriumkarbonat in 60 Teilen Wasser zutropfen. Nachdem alles Trinitroanisol umgesetzt ist, gibt man noch 6 Teile Natriumkarbonat hinzu und erhitzt eine Stunde auf 90 . Der Farbstoff wird durch Aus-salzen abgeschieden und getrock net. 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 brown, well-leveling shades of very good lightfastness, if 1 mole of 3'-methyl-2,6-diaminodiphenylamine-4-sulfonic acid is used with 1 mole. 2.4.6 -Trinitro-l-alkoxybenzene 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> 29; 3 parts of 3'-methyl-2,6-diaminodiphenylamine-4-sulfonic acid, obtained from gon. Densation of 2. 6 - dinitrochlorobenzene - 4 - sulfonic acid with m-toluidine and subsequent reduction of the 1 \ titration groups are dissolved in 500 parts of water until neutral and 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 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 |
---|---|---|---|
DE151162X | 1929-08-17 | ||
CH147460T | 1931-06-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH151162A true CH151162A (en) | 1931-11-30 |
Family
ID=25715030
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH151162D CH151162A (en) | 1929-08-17 | 1930-03-12 | Process for the preparation of a wool dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH151162A (en) |
-
1930
- 1930-03-12 CH CH151162D patent/CH151162A/en unknown
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