1987 Volume 1987 Issue 7 Pages 1475-1478
Dibenzoyl ditelluride [1], tellurium analogue of benzoyl peroxide, was synthesized by the reaction of benzoyl chloride in ether with sodium hydrogentelluride prepared from tellurium and sodium borohydride in water. IR and 13C-NMR spectra of [1] were compared with those of dibenzoyl diselenide [1], selenium analogue [1] reacts with water to give tellurium and benzoic anhydride, and with ethanol to give tellurium and ethyl benzoate by the path (scheme 2), with involves pertellurocarboxylic Te-acid and Tellurocarboxylic Te-acid as intermediates. [1] seems to eliminate tellurium by the reaction with triphenylphosphine.
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