Acid-catalyzed intermolecular rearrangement of N-chlorocarbazole
…, A Quesada P, DJ Dodsworth
Index: Rosa, Michael De; Quesada, Andres P.; Dodsworth, David J. Journal of Organic Chemistry, 1987 , vol. 52, # 2 p. 173 - 175
Full Text: HTML
Citation Number: 12
Abstract
The chlorination of carbazole with sodium hypochlorite in CH2CI2, CHC13, or CCll gave N- chlorocarbazole in 63-95% yield. It rearranged in refluxing methanol to give carbazole, 3- chlorocarbazole, 1-chlorocarbazole, 3, 6-dichlorocarbazole, and 1, 6-dichlorocarbazole. These chlorocarbazoles were formed in an acid-catalyzed intermolecular reaction. In the presence of potassium carbonate dechlorination of N-chlorocarbazole was observed. No ...
Related Articles:
[Bonesi, Sergio M.; Erra-Balsells, Rosa Journal of Heterocyclic Chemistry, 1997 , vol. 34, # 3 p. 877 - 889]
[Bonesi, Sergio M.; Erra-Balsells, Rosa Journal of Heterocyclic Chemistry, 1997 , vol. 34, # 3 p. 877 - 889]