Revisiting the synthesis of aryl nitriles: a pivotal role of CAN
Rakhee Saikia1, Kwihwan Park2, Hayato Masuda2
1Department of Chemical Sciences, Tezpur University, Napaam, Tezpur, Assam Pin-784028, India. utbora@yahoo.co.in ubora@tezu.ernet.in.
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.
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