CH151161A - Process for the preparation of a wool dye. - Google Patents
Process for the preparation of a wool dye.Info
- Publication number
- CH151161A CH151161A CH151161DA CH151161A CH 151161 A CH151161 A CH 151161A CH 151161D A CH151161D A CH 151161DA CH 151161 A CH151161 A CH 151161A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- parts
- wool
- dye
- mol
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- 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-1- chlorbenzol kondensiert.
Hierbei findet zu nächst die zu erwartende Reaktion zwischen dem Chloratom und einer Aminogruppe statt, bei weiterem Erhitzen in Gegenwart von Alkali tritt dann aber unter Abspaltung von Alkalinitrit eine innere Kondensation ein.
Beispiel: 29,3 Teile 3'-Methyl-2.6-diaminodiphe- nylamin-4-sulfosäure, erhalten durch Kon densation von 2. 6 - Dinitrochlorbenzol - 4 - sulfosäure mit m-Toluidin und folgende Re duktion der Nitrogruppen, werden in 500 Teilen Wasser neutral gelöst und bei 70 bis 80 mit 24 Teilen 2. 4. 6-Trinitrochlorben- zol, welches man allmählich unter Rühren zugibt, kondensiert.
Gleichzeitig lässt man eine Lösung von 11 Teilen Natriumkarbonat in 110 Teilen Wasser zutropfea- Nachdem alles Trinitrochlorbenzol umgesetzt ist, gibt man noch 6 Teile Natriumkarbonat hinzu und erhitzt eine Stunde auf 90 . Der Farb stoff 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 brown, well-leveling shades of very good lightfastness, if one mole of 3'-methyl-2. 6-diaminodiphenylamine-4-sulfonic acid condensed with 1 mol. 2.4.6-trinitro-1-chlorobenzene.
In this case, the reaction to be expected 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 elimination of alkali metal nitrite.
Example: 29.3 parts of 3'-methyl-2,6-diaminodiphenylamine-4-sulfonic acid, obtained by condensation of 2.6 - dinitrochlorobenzene - 4 - sulfonic acid with m-toluidine and the following reduction of the nitro groups, are in 500 parts Water dissolved neutrally and at 70 to 80 with 24 parts of 2-4 parts of 6-trinitrochlorobenzene, which is gradually added with stirring, condensed.
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 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 |
---|---|---|---|
DE151161X | 1929-08-17 | ||
CH147460T | 1931-06-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH151161A true CH151161A (en) | 1931-11-30 |
Family
ID=25715029
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH151161D CH151161A (en) | 1929-08-17 | 1930-03-12 | Process for the preparation of a wool dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH151161A (en) |
-
1930
- 1930-03-12 CH CH151161D patent/CH151161A/en unknown
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