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

Rakhee Saikia, Kwihwan Park, Hayato Masuda, Miki Itoh, Tsuyoshi Yamada, Hironao Sajiki, Sanjeev P. Mahanta, Ashim J. Thakur

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

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 CNleading 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.

Original languageEnglish
Pages (from-to)1344-1351
Number of pages8
JournalOrganic and Biomolecular Chemistry
Volume19
Issue number6
DOIs
StatePublished - 2021/02/14

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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