CH158722A - Process for the production of an indigoid vat dye. - Google Patents
Process for the production of an indigoid vat dye.Info
- Publication number
- CH158722A CH158722A CH158722DA CH158722A CH 158722 A CH158722 A CH 158722A CH 158722D A CH158722D A CH 158722DA CH 158722 A CH158722 A CH 158722A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- dye
- indigoid
- vat dye
- naphthisatin
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines indigoiden Y üpenfarbstofes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines indigoiden Nüpenfarbstoffes, dadurch gekennzeichnet, dass man Monobrom-2. 1-Naphtisatin, erhal ten durch Bromieriing" von 2. 1-Naphtisatin, nach Überführung in das a-Chlorid mit 2'-iUethoxy - 6 . 7 - benzo-3-oxy-thionaphthen kondensiert.
Der so erhaltene Farbstoff löst sich in konzentrierter Schwefelsäure mit blauviolet ter Farbe und färbt aus gelber güpe die Faser olive.
<I>Beispiel:</I> 27 Teile Monobrom-2. 1-naphtisatin, das durch Bromieren von 2. 1-Naphtisatin erhal ten wurde, werden durch Erwärmen mit 26 Teilen Phosphorpentachlorid in etwa 400 Teilen Chlorbenzol in das Isatin-a-ohlorid übergeführt. Diese Lösung vereinigt man dann mit einer Lösung von 23 Teilen 2'-Methoxy-6 . 7-benzo-3-oxy-thionaphthen in Chlorbenzol. Man erwärmt noch kurze Zeit auf etwa .80 bis 85 , filtriert den gebildeten Farbstoff ab, wäscht ihn mit Chlorbenzol aus und trocknet.
Process for the production of an indigoid Yupene dye. The present patent relates to a process for the production of an indigoid pebble dye, characterized in that monobromo-2. 1-naphthisatin, obtained by bromination "of 2. 1-naphthisatin, condensed after conversion into the α-chloride with 2'-ethoxy - 6, 7 - benzo-3-oxy-thionaphthene.
The dye obtained in this way dissolves in concentrated sulfuric acid with a blue-violet color and dyes the fiber olive from a yellow güpe.
<I> Example: </I> 27 parts of Monobrom-2. 1-naphtisatin, which was obtained by brominating 2. 1-naphtisatin, is converted into isatin a-chloride by heating with 26 parts of phosphorus pentachloride in about 400 parts of chlorobenzene. This solution is then combined with a solution of 23 parts of 2'-methoxy-6. 7-benzo-3-oxy-thionaphthene in chlorobenzene. The mixture is heated for a short time to about .80 to 85, the dye formed is filtered off, washed out with chlorobenzene and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE158722X | 1930-08-01 | ||
CH155459T | 1931-07-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH158722A true CH158722A (en) | 1932-11-30 |
Family
ID=25716600
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH158722D CH158722A (en) | 1930-08-01 | 1931-07-27 | Process for the production of an indigoid vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH158722A (en) |
-
1931
- 1931-07-27 CH CH158722D patent/CH158722A/en unknown
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