Electrochemical organic reactions via catalytic halide substitut

Chemistry: electrical and wave energy – Processes and products

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204 81, C25B 310

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active

049043706

ABSTRACT:
An improved process for the electrochemical reaction of a lower organic halide, e.g., benzyl chloride, wherein the improvement comprises the catalytic in situ conversion of the lower organic halide to a higher organic halide, e.g., benzyl iodide, which reacts under milder conditions than does the lower organic halide. An example of such an improved process is the dimerization of a benzyl chloride to form a diphenylethane wherein a catalytic amount of sodium iodide is added to the electrochemical cell under conditions such that the conversion of the benzyl chloride to benzyl iodide is effectively driven to completion.

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Girard, P. et al. "Divalent Lanthanide Derivatives in Organic Synthesis: Mild Preparation of SmI2 and YbI2 and Their Use as Reducing or Coupling Agents", Journal of the American Chemical Society, vol. 102, No. 8 (Apr. 1980) pp. 2693-2695.
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