CH116083A - Process for the production of an indigoid dye of the anthracene series. - Google Patents
Process for the production of an indigoid dye of the anthracene series.Info
- Publication number
- CH116083A CH116083A CH116083DA CH116083A CH 116083 A CH116083 A CH 116083A CH 116083D A CH116083D A CH 116083DA CH 116083 A CH116083 A CH 116083A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- anthracene series
- indigoid dye
- dye
- indigoid
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B7/00—Indigoid dyes
- C09B7/10—Bis-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines indigoiden Farbstoffes der Anthracenreilie.. Es wurde gefunden, dass man einen in- digoiden Farbstoff der Anthracenreihe erhält, wenn man ein Anil des 2,3-Anthrachinon- thioisatins mit Ox;ythionaphthenkarbonsäure kondensiert.
Der Farbstoff bildet ein violett schwarzes Pulver, das sich in Schwefelsäure mit grüner Farbe löst und eine schwarz braune Küpe gibt, aus welcher Baumwolle heliotrop gefärbt wird. Beispiel 20,5 Teile des p-Dim,ethylaminoanils des 2,3-Antlirachinonthioisatins werden mit 10 Teilen Oxythionaphthenkarbonsäure und 500 Teilen Pyridin oder Trichlorbenzol zwei Stunden unter Rückfluss gekocht. Der aus geschiedene Farbstoff wird abgesaugt, ge waschen und getrocknet.
Die Reaktion verläuft nach folgender Gleichung:
EMI0001.0021
Process for the production of an indigoid dye of the anthracene series. It has been found that an indigoid dye of the anthracene series is obtained if an anil of 2,3-anthraquinone thioisatin is condensed with oxythionaphthenecarboxylic acid.
The dye forms a purple black powder that dissolves in sulfuric acid with a green color and gives a black-brown vat from which cotton is heliotrope dyed. EXAMPLE 20.5 parts of the p-dim, ethylaminoanil of 2,3-antlirachinonthioisatins are refluxed for two hours with 10 parts of oxythionaphthenecarboxylic acid and 500 parts of pyridine or trichlorobenzene. The separated dye is filtered off, washed and dried.
The reaction proceeds according to the following equation:
EMI0001.0021
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103649T | 1923-01-24 | ||
CH116083T | 1924-06-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH116083A true CH116083A (en) | 1926-08-02 |
Family
ID=25706538
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH116083D CH116083A (en) | 1923-01-24 | 1924-06-21 | Process for the production of an indigoid dye of the anthracene series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH116083A (en) |
-
1924
- 1924-06-21 CH CH116083D patent/CH116083A/en unknown
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