CH135143A - Process for the preparation of a violet vat dye of the 2-thionaphthene-2'-indolindigo series. - Google Patents
Process for the preparation of a violet vat dye of the 2-thionaphthene-2'-indolindigo series.Info
- Publication number
- CH135143A CH135143A CH135143DA CH135143A CH 135143 A CH135143 A CH 135143A CH 135143D A CH135143D A CH 135143DA CH 135143 A CH135143 A CH 135143A
- Authority
- CH
- Switzerland
- Prior art keywords
- thionaphthene
- series
- preparation
- indolindigo
- dye
- Prior art date
Links
Description
Verfahren zur Darstellung eines violetten Küpenfarbstoffes der 2-Thionaphten-2'-indolindigoreihe. Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Darstellung eines vio letten Küpenfarbstoffes der 2-Thionaphten-2'- indolindigo-Reihe der Formel:
EMI0001.0006
den man durch Kondensation von 5-Chlor- 4.7-dimethyl-3-oxy-l-thionaphten mit einer reaktionsfähigen 4,5-Dichlor-7-methylisatin-a- verbindung erhält.
Trocken ist der Farbstoff ein violett gefärbtes Pulver, das in konzen trierter Schwefelsäure blaugrün löslich ist. Mit Natronlauge und Hydrosulfit gibt er eine gelbe Küpe, aus der die Faser echt violett angefärbt wird. <I>Beispiel</I> 23 Gewichtsteile 4,5-Dichlor-7-rnethylisatin werden in etwa 200 Gewichtsteilen Chlor benzol suspendiert und nach Zusatz von 22 Gewichtsteilen Phosphorpentachlorid erhitzt.
Die entstandene Lösung des 4,5-Dichlor-7- methylisatin-a-chlorids wird in eine Lösung von 21,2 Gewichtsteilen 5-Chlor-4,7-dimethyl- 3-oxy-l-tionaphten in 200 Gewichtsteilen Chlorbenzol einlaufen gelassen, wobei sich der Farbstoff sofort abscheidet. Nach kurzem Erwärmen auf 80-90 wird der Farbstoff filtriert, mit Alkohol gewaschen und ge trocknet.
Process for the preparation of a violet vat dye of the 2-thionaphthene-2'-indolindigo series. The present invention relates to a process for the preparation of a violet vat dye of the 2-thionaphthene-2'-indolindigo series of the formula:
EMI0001.0006
which is obtained by condensation of 5-chloro-4,7-dimethyl-3-oxy-1-thionaphthene with a reactive 4,5-dichloro-7-methylisatin-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 a yellow vat from which the fibers are dyed really purple. <I> Example </I> 23 parts by weight of 4,5-dichloro-7-methylisatin 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 4,5-dichloro-7-methylisatin-a-chloride is allowed to run into a solution of 21.2 parts by weight of 5-chloro-4,7-dimethyl-3-oxy-1-ionaphthene in 200 parts by weight of chlorobenzene, the dye separating out immediately. After brief warming to 80-90, the dye is filtered, washed with alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE135143X | 1927-01-03 | ||
CH132316T | 1927-12-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH135143A true CH135143A (en) | 1929-08-31 |
Family
ID=25711851
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH135143D CH135143A (en) | 1927-01-03 | 1927-12-30 | Process for the preparation of a violet vat dye of the 2-thionaphthene-2'-indolindigo series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH135143A (en) |
-
1927
- 1927-12-30 CH CH135143D patent/CH135143A/en unknown
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