CH110414A - Process for the preparation of an anthracene derivative. - Google Patents
Process for the preparation of an anthracene derivative.Info
- Publication number
- CH110414A CH110414A CH110414DA CH110414A CH 110414 A CH110414 A CH 110414A CH 110414D A CH110414D A CH 110414DA CH 110414 A CH110414 A CH 110414A
- Authority
- CH
- Switzerland
- Prior art keywords
- anthracene derivative
- preparation
- acid
- anthracene
- parts
- 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
<B>Zusatzpatent</B> zum Hauptpatent Nr. 103217. Verfahren zur Herstellung eines Anthracenderivates. Es wurde gefunden, dass man ein Anthra- cenderivat, die im Hauptpatent No. 103647 beschriebene 2,3-Anthracenthioglycolkarbon- säure, erhält, wenn man 131o1. 2,3-1VIercapto- anthracenkarbonsäure mit 1 Mol. Chloressig säure in Reaktion bringt.
<I>Beispiel:</I> 25 Teile 2,3-Mercaptoanthracenkarbon- säure, 150 Teile Alkohol, 10 Teile Choressig- s iture werden unter Rühren mit 18 Teilen Aetzkali versetzt. Die zunächst in Lösung gehende Mercaptokarbonsäure kondensiert rasch und fällt als Thioglycolkarbonsäure aus, während die Temperatur bis auf zirka 70 steigt. Nach einstündigem Rühren wird ab gesaugt, mit Alkohol gewaschen, in zirka 500 Teilen Wasser gelöst, kalt filtriert, heiss aasgesäuert, abgesaugt, gewaschen und ge trocknet.
<B> Additional patent </B> to main patent no. 103217. Process for the production of an anthracene derivative. It was found that an anthracene derivative described in main patent no. 2,3-Anthracene thioglycolcarboxylic acid described 103647, is obtained when 131o1. 2,3-1VIercapto-anthracene carboxylic acid with 1 mol. Chloracetic acid in reaction.
<I> Example: </I> 25 parts of 2,3-mercaptoanthracene carboxylic acid, 150 parts of alcohol, 10 parts of chloroacetic acid are mixed with 18 parts of caustic potash while stirring. The mercaptocarboxylic acid, which initially goes into solution, condenses rapidly and precipitates as thioglycol carbonic acid, while the temperature rises to around 70. After stirring for one hour, the product is filtered off with suction, washed with alcohol, dissolved in about 500 parts of water, filtered cold, acidified while hot, filtered off with suction, washed and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103217T | 1923-01-24 | ||
CH110414T | 1924-07-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH110414A true CH110414A (en) | 1925-06-01 |
Family
ID=25706343
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH110414D CH110414A (en) | 1923-01-24 | 1924-07-22 | Process for the preparation of an anthracene derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH110414A (en) |
-
1924
- 1924-07-22 CH CH110414D patent/CH110414A/en unknown
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