CH149715A - Process for the preparation of a vat dye. - Google Patents
Process for the preparation of a vat dye.Info
- Publication number
- CH149715A CH149715A CH149715DA CH149715A CH 149715 A CH149715 A CH 149715A CH 149715D A CH149715D A CH 149715DA CH 149715 A CH149715 A CH 149715A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- dye
- vat
- vat dye
- dyes
- Prior art date
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- Coloring (AREA)
Description
Verfahren zur Darstellung eines Nüpenfarbstoifes. Es wurde gefunden, dass durch Konden sation von 6-Alkoxy-3-oxy-l-thionaphtenen mit substituierten Isatinen von folgender Formel:
EMI0001.0004
a = Halogen oder Alkyl; b = Halogen, Alkyl oder Wasserstoff; c = Halogen, Alkyl oder Wasserstoff; klar orange färbende sehr echte Küpenfarb- stoffe erhalten werden.
Die Farbstoffe zeichnen sieh durch reine Farbtöne und durch besondere Lichtechtheit aus, welche die Lichtechtheit der hochwer tigen, orange färbenden güpenfarbstoffe der Anthrachinonreihe teilweise sogar erreicht. Die neuen Farbstoffe eignen sich mit Vorteil für den Zeugdruck. Für die Kondensation sind die bekannten Ausführungsformen an wendbar.
Gegenstand dieses Patentes ist ein Ver fahren zur Darstellung eines Küpenfarb- stoffes, welches dadurch gekennzeichnet ist, dass man 6-Methoxy-3-oxythionaphten mit 5. 7-Dichlorisatin kondensiert. <I>Beispiel:</I> 18 Gewichtsteile 6-Methoxy-3-oxythio- naphten werden in 200 Gewichtsteilen Eis essig oder Essigsäureanhydrid unter Erwär men gelöst und mit einer Lösung von 22 Ge wichtsteilen 5. 7-Dichlorisatin in 200 Ge wichtsteilen Eisessig vereinigt.
Nach Zugabe von etwas konzentrierter Salzsäure fällt der 6-Methoxy-2-thionaphten-5'-7'-dichlor-3'- indolindigo aus der heissen Lösung in kristal liner Form aus. Durch kurzes Nachrühren auf dem Dampfbad wird die Farbstoffbii- dung beendet. Der Farbstoff wird nach dem Erkalten der Lösung abgesaugt, mit Eisessig und alsdann mit Wasser gewaschen. Er färbt aus gelber Küpe die Faser in klaren orange farbigen Tönen von guter Wasch-, Koch- und Lichtechtheit an.
Process for the representation of a nub dye. It has been found that condensation of 6-alkoxy-3-oxy-l-thionaphtenes with substituted isatins of the following formula:
EMI0001.0004
a = halogen or alkyl; b = halogen, alkyl or hydrogen; c = halogen, alkyl or hydrogen; very genuine vat dyes that give clear orange color are obtained.
The dyes are characterized by pure shades and special lightfastness, which in some cases even achieves the lightfastness of the high-quality, orange-colored quality dyes of the anthraquinone series. The new dyes are advantageously suitable for stuff printing. The known embodiments can be used for the condensation.
The subject of this patent is a process for the preparation of a vat dye which is characterized in that 6-methoxy-3-oxythionaphthene is condensed with 5, 7-dichloroisatin. <I> Example: </I> 18 parts by weight of 6-methoxy-3-oxythio- naphthene are dissolved in 200 parts by weight of glacial acetic acid or acetic anhydride with heating and mixed with a solution of 22 parts by weight of 5,7-dichloroisatin in 200 parts by weight of glacial acetic acid united.
After adding a little concentrated hydrochloric acid, the 6-methoxy-2-thionaphthene-5'-7'-dichloro-3'-indolindigo precipitates out of the hot solution in crystalline form. The dye formation is ended by briefly stirring on the steam bath. After the solution has cooled, the dye is filtered off with suction, washed with glacial acetic acid and then with water. He dyes the fiber from a yellow vat in clear orange shades of good washing, boiling and lightfastness.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE149715X | 1929-09-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH149715A true CH149715A (en) | 1931-09-30 |
Family
ID=5673498
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH149715D CH149715A (en) | 1929-09-25 | 1930-09-24 | Process for the preparation of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH149715A (en) |
-
1930
- 1930-09-24 CH CH149715D patent/CH149715A/en unknown
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