CH119149A - Process for the preparation of an anthracene derivative. - Google Patents
Process for the preparation of an anthracene derivative.Info
- Publication number
- CH119149A CH119149A CH119149DA CH119149A CH 119149 A CH119149 A CH 119149A CH 119149D A CH119149D A CH 119149DA CH 119149 A CH119149 A CH 119149A
- Authority
- CH
- Switzerland
- Prior art keywords
- anthraquinone
- anthracene derivative
- yellow
- preparation
- oxythiophene
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/24—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Anthracenderivates. Es wurde gefunden, dass man ein neues Anthracenderivat, das 2,1-Anthrachinonoxy- thiophen, erhält, wenn man die 2,1-Anthra- chinonthioglykolkarbonsäure mit Konden sationsmitteln behandelt.
Das 2,1-Anthrachinonoxythiophen bildet ein grauviolett gefärbtes Pulver. Es ist mit bräunlichgelber Farbe in Schwefelsäure lös lich und gibt mit Hydrosulfit und Natron lauge eine gelborange Küpe. Es ist ein wertvolles Ausgangsmaterial zur Herstel lung von Farbstoffen.
<I>Beispiel:</I> 1 Teil 2,1-Anthrachinonthioglykolkarbon- säure wird mit 0,2 Teilen entwässertem Na triumacetat in 5 Teilen Essigsäureanhydrid vorsichtig erwärmt, bis die Kohlensäure entwicklung aufgehört hat.
Hierauf destil liert man das Essigsäureanhydrid im Va kuum ab, giesst den Rückstand in Wasser, kocht auf und filtriert die in gelben Flocken ausgeschiedene Azetylverbindung des 2,1- Anthrachinonoxythiophens. Diese wird dann durch Erwärmen mit Alkali in Wasser oder Alkohol verseift, wobei die oliv e Azetylver- bindung in das 2,1-Anthrachinonoxythiophen übergeht.
Process for the preparation of an anthracene derivative. It has been found that a new anthracene derivative, the 2,1-anthraquinone oxythiophene, is obtained if the 2,1-anthraquinone thioglycolic acid is treated with condensation agents.
The 2,1-anthraquinone oxythiophene forms a gray-violet colored powder. It is brownish-yellow in color and soluble in sulfuric acid, and with hydrosulphite and sodium hydroxide solution, it gives a yellow-orange vat. It is a valuable starting material for the manufacture of dyes.
<I> Example: </I> 1 part of 2,1-anthraquinone thioglycolic acid is carefully heated with 0.2 part of dehydrated sodium acetate in 5 parts of acetic anhydride until the development of carbonic acid has stopped.
The acetic anhydride is then distilled off in vacuo, the residue is poured into water, boiled and the acetyl compound of 2,1-anthraquinone oxythiophene which is precipitated in yellow flakes is filtered off. This is then saponified by heating with alkali in water or alcohol, the olive acetyl compound being converted into 2,1-anthraquinone oxythiophene.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103648T | 1923-01-24 | ||
CH119149T | 1925-03-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH119149A true CH119149A (en) | 1927-03-01 |
Family
ID=25706528
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH119149D CH119149A (en) | 1923-01-24 | 1925-03-18 | Process for the preparation of an anthracene derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH119149A (en) |
-
1925
- 1925-03-18 CH CH119149D patent/CH119149A/en unknown
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