CH135126A - 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
- CH135126A CH135126A CH135126DA CH135126A CH 135126 A CH135126 A CH 135126A CH 135126D A CH135126D A CH 135126DA CH 135126 A CH135126 A CH 135126A
- Authority
- CH
- Switzerland
- Prior art keywords
- thionaphthene
- series
- indolindigo
- production
- dye
- Prior art date
Links
Landscapes
- Indole Compounds (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines violetten Küpenfarbstoffes der 2-Thionaphten-2'-Indolindigoreihe. <B>.</B> Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Darstellung eines vio letten Küpenfarbstoffes der 2-Thionaphten- 2'-indolindigoi-eihe der Formel:
EMI0001.0006
dureh Kondensation von 5-chlor-7-methyl-3- oxy-l-thionaphteii mit einerreaktionsfähigen 5- chloi--4.7-dimethylisatioti-a-verbindung. Trok- ken ist der Farbstoff ein violett gefärbtes Pulver, das in konzentrierter Schwefelsäure blaugrün löslich ist. Mit Natronlauge und Hydrosulfit gibt er eine olive Küpe, aus der die Faser echt violett angefärbt wird.
<I>Beispiel:</I> 21 Gewichtsteile 5-Chlor-4.7-dimethylisa- tin werden in etwa 200 Gewichtsteilen Chlor- benzol suspendiert und nach Zusatz von 22 Gewichtsteilen Phosphorpentachlorid erhitzt. Die entstandene Lösung des 5-Chlor-4.7-di- methylisatin-a-chlorids wird in eine Lösung von 20 Gewichtsteilen 5-Chloi--7-niethyl-3- oxy-l-thioi)aphteD in 200 Gewichtsteilen Chlor benzol einlaufen gelassen, wobei sich der Farbstoff sofort abscheidet. Nach kurzem Erwärmen auf<B>80-900 0</B> wird der Farb stoff filtriert, mit Alkohol gewaschen und ge trocknet.
Process for the preparation of a violet vat dye of the 2-thionaphthene-2'-indolindigo series. <B>. </B> The present invention relates to a process for the preparation of a violet vat dye of the 2-thionaphthene-2'-indolindigoi series of the formula:
EMI0001.0006
by condensation of 5-chloro-7-methyl-3-oxy-l-thionaphteii with a reactive 5-chloi - 4.7-dimethylisatioti-a-compound. When dry, the dye is a violet colored powder that is soluble in concentrated sulfuric acid in a blue-green color. With caustic soda and hydrosulphite, he gives an olive vat from which the fiber is dyed really purple.
<I> Example: </I> 21 parts by weight of 5-chloro-4,7-dimethylizine are suspended in about 200 parts by weight of chlorobenzene and heated after adding 22 parts by weight of phosphorus pentachloride. The resulting solution of 5-chloro-4,7-dimethylisatin-a-chloride is allowed to run into a solution of 20 parts by weight of 5-chloro-7-niethyl-3-oxy-1-thioi) aphteD in 200 parts by weight of chlorobenzene, the dye separating out immediately. After briefly warming to <B> 80-900 0 </B>, the dye is filtered, washed with alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE135126X | 1927-01-03 | ||
CH132316T | 1927-12-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH135126A true CH135126A (en) | 1929-08-31 |
Family
ID=25711834
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH135126D CH135126A (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) | CH135126A (en) |
-
1927
- 1927-12-30 CH CH135126D patent/CH135126A/en unknown
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