CH135133A - Process for the production of a violet vat dye of the 2-thionaphthene-2'-indolindigo series. - Google Patents
Process for the production of a violet vat dye of the 2-thionaphthene-2'-indolindigo series.Info
- Publication number
- CH135133A CH135133A CH135133DA CH135133A CH 135133 A CH135133 A CH 135133A CH 135133D A CH135133D A CH 135133DA CH 135133 A CH135133 A CH 135133A
- Authority
- CH
- Switzerland
- Prior art keywords
- thionaphthene
- series
- indolindigo
- production
- dye
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines violetten Kirpenfarbstoä%s der 2-Tiiionapiiten-2'-indolindigoreihe. Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Darstellung eines vio letten Küpenfarbstoffes der 2-Thionapliten-2'- indolindigoreihe der Formel:
EMI0001.0007
den man durch Kondensation von 4-DIethyl- 6-chlor--oxy-l-thionaphten mit einer reak tionsfähigen 4. 5 . 7-Trimethylisatin-a-verbin- dung erhält. Trocken ist der Farbstoff ein violettrot gefärbtes Pulver, das in konzen trierter Schwefelsäure blaugrün löslich ist. i51it Natronlauge und Hydrosulfit gibt er eine gelbe Küpe, aus der die Faser echt violettrot angefärbt wird.
<I>Beispiel:</I> 19 Gewichtsteile 4 . 5 . 7-Trimethylisatin weiden in etwa 200 Gewichtsteilen Chlor benzol suspendiert und nach Zusatz von 22 Gewichtsteilen Phosphorpentachlorid erhitzt. Die entstandene Lösung des 4. b.7-Trimethyl- isatiri-a-chlorids wird in eine Lösung von 20 Gewichtsteilen 4-I4lethyl-6-chlor-3-ogy-l-thio- naphteti in 200 Gewichtsteile Chlorbenzol einlaufen gelassen, wobei sich der Farbstoff sofort abscheidet. Nach kurzem Erwärmen auf<B>80-90"</B> wird der Farbstoff filtriert, mit Alkohol gewaschen und getrocknet.
Process for the production of a purple cherry color of the 2-Tiiionapiiten-2'-indolindigo series. The present invention relates to a process for the preparation of a violet vat dye of the 2-thionaplite-2'-indolindigo series of the formula:
EMI0001.0007
which is obtained by condensation of 4-DIethyl-6-chloro-oxy-l-thionaphthene with a reactive 4. 5. 7-trimethylisatin-α-compound is obtained. When dry, the dye is a violet-red colored powder that is soluble in concentrated sulfuric acid in a blue-green color. With caustic soda and hydrosulphite, he gives a yellow vat from which the fibers are stained real purple-red.
<I> Example: </I> 19 parts by weight 4. 5. 7-Trimethylisatin is suspended in about 200 parts by weight of chlorine benzene and heated after adding 22 parts by weight of phosphorus pentachloride. The resulting solution of 4. b.7-trimethyl-isatiri-a-chloride is allowed to run into a solution of 20 parts by weight of 4-14lethyl-6-chloro-3-ogy-1-thio-naphtheti in 200 parts by weight of chlorobenzene, whereby the dye separates out immediately. After briefly heating to <B> 80-90 "</B>, the dye is filtered, washed with alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE135133X | 1927-01-03 | ||
CH132316T | 1927-12-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH135133A true CH135133A (en) | 1929-08-31 |
Family
ID=25711841
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH135133D CH135133A (en) | 1927-01-03 | 1927-12-30 | Process for the production of a violet vat dye of the 2-thionaphthene-2'-indolindigo series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH135133A (en) |
-
1927
- 1927-12-30 CH CH135133D patent/CH135133A/en unknown
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