CH146444A - Process for the preparation of 5.6.7-trichloro- (2) -thionaphten-4'-chloro-7'-methoxy- (2 ') -indole-indigo. - Google Patents
Process for the preparation of 5.6.7-trichloro- (2) -thionaphten-4'-chloro-7'-methoxy- (2 ') -indole-indigo.Info
- Publication number
- CH146444A CH146444A CH146444DA CH146444A CH 146444 A CH146444 A CH 146444A CH 146444D A CH146444D A CH 146444DA CH 146444 A CH146444 A CH 146444A
- Authority
- CH
- Switzerland
- Prior art keywords
- trichloro
- chloro
- thionaphten
- methoxy
- indigo
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung von 5.6.7-Trichlor-(2)-thionaphteii-4'-chlor- 7 <B>9</B> .mothoxy-(2')-.indol-indigo. Gegenstand dieses Patentes ist ein Ver fahren zur Darstellung von 5.6.7-Trichlor- (2)-thionaphten-4'-chlor-7'-methoxy- (2') -indol- indigo, welches dadurch gekennzeichnet ist, dass man 5.6.7-Trichlor-3-oxy-thionaphten in Gegenwart eines indifferenten organischen Lösungsmittels mit einem reaktionsfähigen a-Derivat des 4-Chlor-7-methoxy-isatins kon densiert.
<I>Beispiel:</I> Mai) bereitet eine Lösung von 4-Chlor-7- methoxy-isatin-a-chlorid und kondensiert dieses mit 25 Teilen 5.6.7-Trichlor-3-oxy- ihionaphten, gelöst in 200 Teilen Chlorbenzol in der üblichen Weise. Der so erhaltene Farbstoff löst sich in konzentrierter Schwefel säure mit blaugrüner Farbe. Die Baumwoll- faser wird aus orangegelber Hydrosulfitküpe rein blau angefärbt. Die Farbe ist grünsti- chiger als die des Farbstoffes des Zusatz patentes Nr. 145895.
Process for the preparation of 5.6.7-trichloro- (2) -thionaphteii-4'-chloro-7 <B> 9 </B> .mothoxy- (2 ') -. Indole-indigo. The subject of this patent is a process for the preparation of 5.6.7-trichloro (2) -thionaphten-4'-chloro-7'-methoxy- (2 ') -indole indigo, which is characterized in that one 5.6. 7-Trichloro-3-oxy-thionaphthene condenses in the presence of an inert organic solvent with a reactive α-derivative of 4-chloro-7-methoxy-isatin.
<I> Example: </I> Mai) prepares a solution of 4-chloro-7-methoxy-isatin-a-chloride and condenses this with 25 parts of 5.6.7-trichloro-3-oxy-ihionaphten, dissolved in 200 parts Chlorobenzene in the usual way. The dye thus obtained dissolves in concentrated sulfuric acid with a blue-green color. The cotton fiber is dyed pure blue from an orange-yellow hydrosulfite vat. The color is greener than that of the dye of the additional patent no. 145895.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE146444X | 1928-04-07 | ||
| CH143034T | 1929-04-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH146444A true CH146444A (en) | 1931-04-15 |
Family
ID=25714218
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH146444D CH146444A (en) | 1928-04-07 | 1929-04-04 | Process for the preparation of 5.6.7-trichloro- (2) -thionaphten-4'-chloro-7'-methoxy- (2 ') -indole-indigo. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH146444A (en) |
-
1929
- 1929-04-04 CH CH146444D patent/CH146444A/en unknown
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