CH144868A - Process for the preparation of a nitrogenous vat dye. - Google Patents
Process for the preparation of a nitrogenous vat dye.Info
- Publication number
- CH144868A CH144868A CH144868DA CH144868A CH 144868 A CH144868 A CH 144868A CH 144868D A CH144868D A CH 144868DA CH 144868 A CH144868 A CH 144868A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- dye
- nitrogenous
- vat dye
- vat
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfabren zur Darstellung eines stielistoffhaltigen ltüpenfarbstoffes. Es wurde gefunden, dass man einen neuen, wertvollen, stickstoffhaltigen Küpenfarbstoff erhält, wenn man ein in der Bzl-Stellung negativ substituiertes 2. N-Pyrazolanthronyl- benzanthron (erhalten zum Beispiel durch Kondensation von Pyrazolanthron mit einem in Bzl-Stellung negativ substituierten 2- Halogenbenzanthron) mit einem alkalischen Kondensationsmittel behandelt.
Hierbei wird der in Bzl-Stellung befindliche negative Sub- stituent abgespalten.
Der erhaltene Farbstoff löst sich in kon zentrierter Schwefelsäure mit blauer Farbe und färbt Baumwolle aus blauer Küpe in klaren rotstichig violetten Tönen.
Beispiel: 20 Teile 2-N-Pyrazolanthronyl-Bzl-nitro- benzanthron, erhalten zumBeispiel durch Kon densation von 2-Chlor-Bzl-nitrobenzanthron (hellbraune Blättchen aus Nitrobenzol), werden in eine 110 C heisse Mischung von <B>200</B> Teilen Ätzkali und 200 Teilen Äthyl- alkohol eingetragen. Man rührt so lange bei dieser Temperatur, bis die Farbstoffbildung beendet ist. Der Farbstoff wird durch Ein giessen der Schmelze in Wasser und Einlei ten von Luft in die alkalische Flüssigkeit in der üblichen Weise aufgearbeitet.
Procedure for the representation of an oiltip dye containing stems. It has been found that a new, valuable, nitrogen-containing vat dye is obtained if a second N-pyrazolanthronylbenzanthrone which is negatively substituted in the Bzl position (obtained, for example, by condensation of pyrazolanthrone with a 2- Halobenzanthrone) treated with an alkaline condensing agent.
The negative substituent in the Bzl position is split off here.
The dye obtained dissolves in concentrated sulfuric acid with a blue color and dyes cotton from a blue vat in clear reddish violet shades.
Example: 20 parts of 2-N-pyrazolanthronyl-Bzl-nitrobenzanthrone, obtained for example by condensation of 2-chloro-Bzl-nitrobenzanthrone (light brown flakes from nitrobenzene), are poured into a 110 C hot mixture of <B> 200 </ B> parts of caustic potash and 200 parts of ethyl alcohol entered. The mixture is stirred at this temperature until the formation of the dye has ended. The dye is worked up in the usual way by pouring the melt into water and introducing air into the alkaline liquid.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE144868X | 1928-11-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH144868A true CH144868A (en) | 1931-01-31 |
Family
ID=5670449
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH144868D CH144868A (en) | 1928-11-13 | 1929-09-28 | Process for the preparation of a nitrogenous vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH144868A (en) |
-
1929
- 1929-09-28 CH CH144868D patent/CH144868A/en unknown
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