CH116086A - 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
- CH116086A CH116086A CH116086DA CH116086A CH 116086 A CH116086 A CH 116086A CH 116086D A CH116086D A CH 116086DA CH 116086 A CH116086 A CH 116086A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- production
- indigoid dye
- series
- brominated
- 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
- C09B7/06—Indone-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines indigolden Farbstoffes der Aiithracenreihe. Es wurde gefunden, dass man einen in- digoiden Farbstoff der Antliracenreihe erhält, wenn man ein Anil des 2,3-Anthrachinoni- satins mit Oxythionaphthenkar#b#onsnure kon densiert und hierauf den erhaltenen Farbstoff bromiert. Der neue Farbstoff bildet ein rot violettes Pulver,
das sich in Schwefelsäure mit grüner Farbe löst und eine olive Küpe gibt, aus welcher Baumwolle rötlichhelio- trop gefärbt wird.
<I>Beispiel</I> <B>20,5</B> Teile des p-Dimethylaminoanils des 92,3-Ant'hrae,hinonisatins werden mit<B>10</B> Tei- len Oxythionaplithenkarbonsäure und<B>500</B> Teilen Pyridin oder Trichlorbenzol zwei Stunden unter Rückfluss gekocht. Der ausge schiedene Farbstoff wird, abgesaugt, gewa schen und getrocknet.
4 Teile des so erhaltenen Farbstoffes wer den in<B>100</B> Teile Schwefelsäuremonohydrat eingetragen, mit<B>3</B> Teilen Brom versetzt und sechs Stunden kalt gerührt. Hierauf wird. die Reaktionsmasse in Wasser ausgetragen, der abgeschiedene bromierte Farbstoff fil triert und getrocknet.
Die Reaktion in der ersten Phase ver läuft nach folgender Gleichung:
EMI0001.0026
Process for the production of an indigolden dye of the aiithracene series. It has been found that an indigo dyestuff of the anti-liracene series is obtained if an anil of 2,3-anthraquinonisatin is condensed with oxythionaphthenic acid and the dyestuff obtained is then brominated. The new dye forms a red purple powder,
which dissolves in sulfuric acid with a green color and gives an olive vat from which cotton is dyed reddish heliotrope.
<I> Example </I> <B> 20.5 </B> parts of the p-dimethylaminoanil of 92,3-Ant'hrae, hinonisatins with <B> 10 </B> parts of oxythionaplithene carboxylic acid and <B > 500 parts of pyridine or trichlorobenzene boiled under reflux for two hours. The separated dye is filtered off, washed and dried.
4 parts of the dye thus obtained are added to 100 parts of sulfuric acid monohydrate, 3 parts of bromine are added and the mixture is stirred while cold for six hours. Then will. the reaction mass discharged into water, the deposited brominated dye fil trated and dried.
The reaction in the first phase proceeds according to the following equation:
EMI0001.0026
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103649T | 1923-01-24 | ||
CH116086T | 1924-06-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH116086A true CH116086A (en) | 1926-08-02 |
Family
ID=25706541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH116086D CH116086A (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) | CH116086A (en) |
-
1924
- 1924-06-21 CH CH116086D patent/CH116086A/en unknown
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