4.4 Article

Organocatalytic peroxidation of malonates, β-ketoesters, and cyanoacetic esters using n-Bu4NI/t-BuOOH-mediated intermolecular oxidative C(sp3)-O coupling

Journal

TETRAHEDRON
Volume 71, Issue 47, Pages 8985-8990

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2015.09.047

Keywords

Peroxides; Oxidative coupling; Organocatalysis; Malonates; Tetra-n-butylammonium iodide

Funding

  1. Russian Science Foundation [14-23-00150]
  2. Russian Science Foundation [14-23-00150] Funding Source: Russian Science Foundation

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A new organocatalytic approach for the synthesis of peroxides based on CH activation of a sp(3)-hybridized carbon atom is reported. Peroxides were prepared in 31-89% yield by the reaction of malonates, beta-ketoesters, and cyanoacetic esters with a Bu4NI/tert-butyl hydroperoxide system. The formation of the expected hydroxylation products was not observed. In the discovered reaction, tert-butyl hydroperoxide plays a dual role by acting as the oxidant and the O-reagent for the C-O coupling. The synthesis can be scaled up to generate gram quantities of the target products. (C) 2015 Elsevier Ltd. All rights reserved.

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