Density Functional Theory Study of the Mechanisms of Iron-Catalyzed Intramolecular C–H Amination [1,2]-Shift Tandem Reactions of Aryl Azides

• Published in: Organometallics Vol. 34; no. 6; pp. 1129 - 1136
• Main Authors: Ren, Qinghua, Shen, Xiaoyan, Wan, Jinyu, Fang, Jianhui
• Format: Journal Article
• Language: English
• Published: American Chemical Society 23.03.2015
• ISSN: 0276-7333; 1520-6041
• DOI: 10.1021/acs.organomet.5b00087

The mechanisms of iron(II) bromide-catalyzed intramolecular C–H bond amination [1,2]-shift tandem reactions of aryl azides have been studied using density functional theory calculations. The tandem reaction from R 1 , 1-azido-2-(1-methoxy-2-methylpropan-2-yl)benzene, to produce P 2 , 2,3-dimethyl-1H-indole, was calculated. Our results showed that the overall catalytic cycle includes the following steps: (I) extrusion of N2 to form iron nitrene; (II) C–H bond amination; (III) formation of the middle product P 1 , 2-methoxy-3,3-dimethylindoline; (IV) iminium ion formation ; (V) [1,2]-shift process; and (VI) formation of indole P 2 . The rate-limiting step is the [1,2]-shift process, where the energy barrier ΔE = 28.7 kcal/mol in the gas phase. Our calculated results also indicated that the preference for the [1,2]-shift component of the tandem reaction is methyl < ethyl.