CH110416A - Process for the preparation of an anthracene derivative. - Google Patents
Process for the preparation of an anthracene derivative.Info
- Publication number
- CH110416A CH110416A CH110416DA CH110416A CH 110416 A CH110416 A CH 110416A CH 110416D A CH110416D A CH 110416DA CH 110416 A CH110416 A CH 110416A
- Authority
- CH
- Switzerland
- Prior art keywords
- anthracene derivative
- yellow
- anthraquinone
- brown
- preparation
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
verfahren zur .Herstellung eines Anthraeenderivates. Es wurde gefunden; dass man ein neues Anthracenderivat enthält, wenn man ein An- thrachinon-2-glyzin-3-karbonsäure mit Kon densationsmitteln behandelt.
Das neue Anthracenderivat, das als ein Abkömmling des 2,3-Anthrachinonindoxyls aufzufassen ist, bildet bräunlichgelbe Kristalle, welche sich in kalter, konzentrierter Schwefel säure mit orangeroter Farbe lösen und mit Wasser als grünlichgelbe Flocken ausgefällt werden. In Nitrobenzol ist es mit gelbbrauner Farbe löslich. Mit Hydrosulfit und Natron lauge entsteht eine Küpe, die zunächst braun ist und nach einiger Zeit nach olivegrün um schlägt. Es bildet ein wertvolles Ausgangs material zur Darstellung von Farbstoffen.
Beispiel: 29 Teile Arithrachinon-2-glyzin-3-karbon- säure und 15. Teile entwässertes Natrium acetat werden in 290 Teilen Essigsäurean- hydrid einige Zeit rückfliessend gekocht. Vor übergehend entsteht eine .braune Lösung, woraus sich nach kurzer Zeit bräunlichgelbe Kristalle' abscheiden. Diese werden nach dem Erkalten abgesaugt, zuerst mit Eisessig, dann mit Wasser gewaschen und getrocknet.
process for .production of an anthraeene derivative. It was found; that one contains a new anthracene derivative if one treats an anthrachinone-2-glycine-3-carboxylic acid with condensation agents.
The new anthracene derivative, which is to be understood as a derivative of 2,3-anthraquinone indoxyl, forms brownish-yellow crystals, which dissolve in cold, concentrated sulfuric acid with an orange-red color and are precipitated as greenish-yellow flakes with water. It is soluble in nitrobenzene with a yellow-brown color. With hydrosulphite and caustic soda, a vat is created that is initially brown and then turns olive-green after a while. It is a valuable starting material for the representation of dyes.
Example: 29 parts of arithraquinone-2-glycine-3-carbonic acid and 15 parts of dehydrated sodium acetate are refluxed for some time in 290 parts of acetic anhydride. A "brown solution" is formed before a transition, from which brownish-yellow crystals separate out after a short time. After cooling, these are suctioned off, washed first with glacial acetic acid, then with water and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103648T | 1923-01-24 | ||
CH110416T | 1923-11-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH110416A true CH110416A (en) | 1925-06-01 |
Family
ID=25706525
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH110416D CH110416A (en) | 1923-01-24 | 1923-11-30 | Process for the preparation of an anthracene derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH110416A (en) |
-
1923
- 1923-11-30 CH CH110416D patent/CH110416A/en unknown
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