CH140094A - Process for the preparation of a carbazole derivative. - Google Patents
Process for the preparation of a carbazole derivative.Info
- Publication number
- CH140094A CH140094A CH140094DA CH140094A CH 140094 A CH140094 A CH 140094A CH 140094D A CH140094D A CH 140094DA CH 140094 A CH140094 A CH 140094A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- carbazole derivative
- dioxycarbazole
- carbazole
- recrystallization
- Prior art date
Links
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- Indole Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
Verfahren zur Darstellung eines Karbazolderivates. Gegenstand vorliegender Erfindung ist ein Verfahren zur Darstellung eines Karbazolderivates, dadurch gekennzeiehnet, dass man 1.8-Dioxykarbazol-3.6-disulfosäure finit Hilfe einer Mineralsäure unter Druck bei Temperaturen von 170-180 o C in das 1. 8- Dioxykarbazol überführt.
<I>Beispiel:</I> 100 gr 1.8-Dioxykarbazol-3. 6-disulfosaures Kalium, hergestellt zum Beispiel nach DRP 224952, werden in 1400 cm,' 7 o/oiger Schwe felsäure gelöst und 6 Stunden im Autoklav bei 170-180 o Innentemperatur unter Rühren erhitzt. Nach Erkalten wird das in langen schwach bräunlich gefärbten Nadeln aus kristallisierte Reaktionsprodukt abgesaugt und neutral gewaschen.
Das so erhaltene 1.8- Dioxycarbazol ist fast schmelzpunktrein. Zur Analyse wird es durch Umkristallisation aus Toluol in langen Nadeln vom Schmelzpunkt 211-212 o erhalten.
Process for the preparation of a carbazole derivative. The present invention relates to a process for the preparation of a carbazole derivative, characterized in that 1,8-dioxycarbazole-3,6-disulfonic acid is converted into 1,8-dioxycarbazole with the aid of a mineral acid under pressure at temperatures of 170-180 ° C.
<I> Example: </I> 100 gr 1.8-Dioxykarbazol-3. Potassium 6-disulphonate, produced for example according to DRP 224952, is dissolved in 1400 cm, 7% sulfuric acid and heated for 6 hours in an autoclave at an internal temperature of 170-180 ° while stirring. After cooling, the reaction product, which has crystallized from long, pale brownish needles, is filtered off with suction and washed neutral.
The 1,8-dioxycarbazole obtained in this way is almost pure at the melting point. For analysis it is obtained by recrystallization from toluene in long needles with a melting point of 211-212 o.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE140094X | 1928-01-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH140094A true CH140094A (en) | 1930-05-31 |
Family
ID=5668063
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH140094D CH140094A (en) | 1928-01-02 | 1928-08-30 | Process for the preparation of a carbazole derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH140094A (en) |
-
1928
- 1928-08-30 CH CH140094D patent/CH140094A/en unknown
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