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Revisiting the synthesis of aryl nitriles: a pivotal role of CAN

Authors :
Utpal Bora
Kwihwan Park
Tsuyoshi Yamada
Miki Itoh
Ashim Jyoti Thakur
Sanjeev P. Mahanta
Hironao Sajiki
Rakhee Saikia
Hayato Masuda
Source :
Organic & Biomolecular Chemistry. 19:1344-1351
Publication Year :
2021
Publisher :
Royal Society of Chemistry (RSC), 2021.

Abstract

Facilitated by the dual role of Ceric Ammonium Nitrate (CAN), herein we report a cost-effective approach for the cyanation of aryl iodides/bromides with CAN-DMF as an addition to the existing pool of combined cyanation sources. In addition to being an oxidant, CAN acts as a source of nitrogen in our protocol. The reaction is catalyzed by a readily available Cu(ii) salt and the ability of CAN to generate ammonia in the reaction medium is utilized to eliminate the additional requirement of a nitrogen source, ligand, additive or toxic reagents. The mechanistic study suggests an evolution of CN- leading to the synthesis of a variety of aryl nitriles in moderate to good yields. The proposed mechanism is supported by a series of control reactions and labeling experiments.

Details

ISSN :
14770539 and 14770520
Volume :
19
Database :
OpenAIRE
Journal :
Organic & Biomolecular Chemistry
Accession number :
edsair.doi.dedup.....8987104c9984051f56a91d6b82133f15
Full Text :
https://doi.org/10.1039/d0ob02518f