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Issue 3, 2017
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Mechanism of selective C–H cyanation of 2-phenylpyridine with benzyl nitrile catalyzed by CuBr: a DFT investigation

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Abstract

The mechanism of selective C–H cyanation of 2-phenylpyridine catalyzed by CuBr was investigated using the DFT method at the B3LYP/6-31+G(d,p) level, and the integral equation formalism polarized continuum model (IEFPCM) was applied to simulate the solvent effect. The computational results suggested that 2-phenylacetonitrile can convert into benzoyl cyanide under O2 conditions via two paths (a and b), and also, 2-phenylacetonitrile can first react with the O2 anion to yield 2-hydroxy-2-phenylacetonitrile, and then 2-hydroxy-2-phenylacetonitrile goes through oxidative dehydrogenation to yield benzoyl cyanide via four different paths (c, d, e and f). The other part reaction of the conversion of 2-phenylpyridine to 2-(pyridin-2-yl)-benzonitrile catalyzed by CuBr can go through three paths (g, h and i) which involve the coordination of CN and the N atom of 2-phenylpyridine with Cu cations, and then the processes of addition and oxydehydrogenation reactions lead to the final product 2-(pyridin-2-yl)benzonitrile. In addition, another path (j) without the participation of CuBr could also occur. The results could provide valuable insights into these types of interactions and related ones.

Graphical abstract: Mechanism of selective C–H cyanation of 2-phenylpyridine with benzyl nitrile catalyzed by CuBr: a DFT investigation

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Article information


Submitted
23 Oct 2016
Accepted
09 Dec 2016
First published
12 Dec 2016

Org. Chem. Front., 2017,4, 377-385
Article type
Research Article

Mechanism of selective C–H cyanation of 2-phenylpyridine with benzyl nitrile catalyzed by CuBr: a DFT investigation

D. Zhou, F. Yang, X. Yang, C. Yan, P. Zhou and H. Jing, Org. Chem. Front., 2017, 4, 377
DOI: 10.1039/C6QO00652C

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