| Zincke reaction | |
|---|---|
| Named after | Theodor Zincke |
| Reaction type | Coupling reaction |
The Zincke reaction is an organic reaction, named after Theodor Zincke, in which a pyridine is transformed into a pyridinium salt by reaction with 2,4-dinitro-chlorobenzene and a primary amine.[1][2][3][4]
The Zincke reaction should not be confused with the Zincke-Suhl reaction or the Zincke nitration. Furthermore, the Zincke reaction has nothing to do with the chemical element zinc.
- ^ Zincke, Th. (1904). "Ueber Dinitrophenylpyridiniumchlorid und dessen Umwandlungsproducte". Justus Liebigs Annalen der Chemie. 330 (2): 361–374. doi:10.1002/jlac.19043300217.
- ^ Zincke, Th.; Heuser, G.; Möller, W. (1904). "I. Ueber Dinitrophenylpyridiniumchlorid und dessen Umwandlungsproducte". Justus Liebigs Annalen der Chemie. 333 (2–3): 296–345. doi:10.1002/jlac.19043330212.
- ^ Zincke, Th.; Weißpfenning, G. (1913). "Über Dinitrophenylisochinoliniumchlorid und dessen Umwandlungsprodukte". Justus Liebigs Annalen der Chemie. 396 (1): 103–131. doi:10.1002/jlac.19133960107.
- ^ Zincke, Th.; Würker, W. (1904). "Ueber Dinitrophenylpyridiniumchlorid und dessen Umwandlungsproducte". Justus Liebigs Annalen der Chemie. 338: 107–141. doi:10.1002/jlac.19043380107.