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Synlett 2000; 2000(7): 0999-1000
DOI: 10.1055/s-2000-6686
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Electrochemical Fluorodeiodination of Alkyl Iodides

Masanori Sawaguchi* , Shinichi Ayuba, Yutaka Nakamura, Tsuyoshi Fukuhara, Shoji Hara, Norihiko Yoneda
  • *Division of Molecular Chemistry, Graduate School of Engineering, Hokkaido University, Sapporo 060-8628, Japan; Fax +81-11-7 06-65 56; E-mail: Hara@org-mc.eng.hokudai.ac.jp
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Publication Date:
31 December 2000 (online)

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Electrochemical oxidation of alkyl iodides using Et3N-nHF complexes as an electrolyte proceeds under mild conditions to give alkyl fluorides in good yields. The reaction is highly chemoselective and the functional groups in the substrate such as an ester, ketone, chloride, and tosylate could be tolerated under the reaction conditions.

chemoselective reaction - alkyl fluoride - alkyl iodide - electrochemical oxidation

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