CH119633A - 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
- CH119633A CH119633A CH119633DA CH119633A CH 119633 A CH119633 A CH 119633A CH 119633D A CH119633D A CH 119633DA CH 119633 A CH119633 A CH 119633A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- anthracene
- dye
- indigoid dye
- anthracene series
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Description
Verfahren zur Herstellung eines indigoiden Farbstoffes der Anthracenreihe. Es wurde gefunden, dass man einen neuen indigoiden Farbstoff der Anthracenreihe er hält, wenn man das 1,2-Anthracenoxythio- phen mit einem reaktionsfähigen a-Derivat des 7-Methylisatins, wie 7-Methylisatin-a- toluidid oder 7-Methylisatin-a-chlorid, kon densiert.
Der neue Farbstoff ist in Schwefel säure mit grünblauer Farbe löslich, er bildet mit Hydrosulfit und Natronlauge eine braune Küpe, aus welcher Baumwolle in ech ten violetten Tönen gefärbt wird.
<I>Beispiel:</I> <B>25</B> Teile 1,2-Anthracenoxythiophen wer den mit 30 Teilen 7-Methylisatin-a-toluidid in 1000 Teilen Toluol zwei Stunden unter Rückfluss gekocht. Der ausgeschiedene Farb stoff wird abgesaugt, gewaschen und ge trocknet.
Derselbe Farbstoff entsteht auch, wenn man statt der Oxythiophenverbindung die entsprechende Thioglykolkarbonsäure ver wendet. In diesem Falle arbeitet man in Gegenwart von Essigsäureanhy drill und Na triumacetat, wobei die Oxythiophenverbin- dung zunächst entsteht und dann mit den vorhandenen Komponenten reagiert.
Process for the production of an indigoid dye of the anthracene series. It has been found that a new indigoid dye of the anthracene series is obtained when 1,2-anthracene oxythiophene is used with a reactive α-derivative of 7-methylisatin, such as 7-methylisatin-atoluidide or 7-methylisatin-a chloride, condensed.
The new dye is soluble in sulfuric acid with a green-blue color, it forms a brown vat with hydrosulfite and sodium hydroxide solution, from which cotton is dyed in real violet tones.
<I> Example: </I> <B> 25 </B> parts of 1,2-anthracene oxythiophene are refluxed with 30 parts of 7-methylisatin-a-toluidide in 1000 parts of toluene for two hours. The precipitated dye is filtered off with suction, washed and dried.
The same dye is also produced if the corresponding thioglycolic acid is used instead of the oxythiophene compound. In this case, one works in the presence of acetic anhydride and sodium acetate, the oxythiophene compound initially being formed and then reacting with the components present.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103649T | 1923-01-24 | ||
CH119633T | 1925-03-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH119633A true CH119633A (en) | 1927-04-01 |
Family
ID=25706549
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH119633D CH119633A (en) | 1923-01-24 | 1925-03-18 | Process for the production of an indigoid dye of the anthracene series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH119633A (en) |
-
1925
- 1925-03-18 CH CH119633D patent/CH119633A/en unknown
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