Denitrative Cyanation of Nitroalkanes by Nucleophilic Substitution through Anion–Radical Coupling
Abstract We report a photocatalytic denitrative cyanation to directly convert nitroalkanes into nitriles under mild conditions. The reaction proceeds rapidly under blue LED irradiation and exhibits broad functional-group tolerance. Mechanistic investigations support an anion–radical coupling pathway between an α-nitro radical and a cyanide ion. In this mechanism, a nitronate ion undergoes single-electron oxidation to generate an α-nitro radical, which is intercepted by a cyanide ion to form an α-nitronitrile radical anion. Subsequent extrusion of a nitrite ion affords an α-cyano radical, which undergoes reduction and protonation to deliver a nitrile product. This transformation features a distinctive radical anion intermediate that transiently incorporates both a nucleophile and a leaving group, providing a new conceptual platform for the nucleophilic substitution of nitroalkanes.
Authors
- Yoshiaki Nakao (ORCID: https://orcid.org/0000-0003-4864-3761)
- Ayumi Osawa (ORCID: https://orcid.org/0000-0002-5459-3660)
- K Uemura
Institutions
- Kyushu Kyoritsu University (JP)
- Kyushu University (JP)
- Kyoto University (JP)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-09-04
- DOI
- https://doi.org/10.1021/jacs.6c07079
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00