CH120705A - Process for the preparation of an anthracene derivative. - Google Patents
Process for the preparation of an anthracene derivative.Info
- Publication number
- CH120705A CH120705A CH120705DA CH120705A CH 120705 A CH120705 A CH 120705A CH 120705D A CH120705D A CH 120705DA CH 120705 A CH120705 A CH 120705A
- Authority
- CH
- Switzerland
- Prior art keywords
- anthracene
- carboxylic acid
- anthracene derivative
- acid
- preparation
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
- C07C2603/24—Anthracenes; Hydrogenated anthracenes
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Anthracenderivates. Es wurde gefunden, dass man ein neues Anthracenderivat, die Anthracen- 2-thio- glykol-l-karbonsäure, erhält, wenn man auf die 2,1-Merkaptoanthracenkarbonsäure eine Monohalogenessigsäure einwirken lässt. Die Anthracen-2-thioglykol-l-karbonsäure bildet 'ein hellgelbes Pulver, sie löst sich in Soda lösung mit bräunlichgelber, in konzentrier ter Schwefelsäure mit braunroter, bald nach braun umschlagender Farbe.
Die neue Ver bindung wird zur Herstellung von Farbstof fen verwendet.
<I>Beispiel:</I> 12 Teile 2,.1-Merkaptoanthracenkarbon- säure, 70 Teile Alkohol und 5 Teile Mono chloressigsäure werden zusammen nach Zu gabe von 8: Teilen Kalihydrat einige Zeit gerührt. Hierauf wird die klare Lösung mit konzentrierter Salzsäure sauer gestellt, von ausgeschiedenen anorganischen Salzen und Nebenprodukten filtriert, der Alkohol im Vakuum verdampft, der Rückstand mit Sodalösung extrahiert und das alkalische Ex trakt nusgesäuert. .
Process for the preparation of an anthracene derivative. It has been found that a new anthracene derivative, anthracene-2-thioglycol-1-carboxylic acid, is obtained if a monohaloacetic acid is allowed to act on the 2,1-mercaptoanthracene carboxylic acid. The anthracene-2-thioglycol-1-carboxylic acid forms a pale yellow powder, it dissolves in soda solution with a brownish-yellow, in concentrated sulfuric acid with a brownish-red color, soon turning brown.
The new compound is used to make dyes.
<I> Example: </I> 12 parts of 2,1-mercaptoanthracenecarboxylic acid, 70 parts of alcohol and 5 parts of monochloroacetic acid are stirred together for some time after adding 8 parts of potassium hydrate. The clear solution is then acidified with concentrated hydrochloric acid, the precipitated inorganic salts and by-products are filtered off, the alcohol is evaporated in vacuo, the residue is extracted with soda solution and the alkaline extract is acidified with a nut. .
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103217T | 1923-01-24 | ||
CH120705T | 1925-03-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH120705A true CH120705A (en) | 1927-06-01 |
Family
ID=25706346
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH120705D CH120705A (en) | 1923-01-24 | 1925-03-18 | Process for the preparation of an anthracene derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH120705A (en) |
-
1925
- 1925-03-18 CH CH120705D patent/CH120705A/en unknown
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