Stereoselective Electrochemical Synthesis of E‐Tetrasubstituted Haloalkenyl Chalcogenides

Herein, we describe an electrochemical method for the synthesis of haloalkenyl chalcogenides from internal alkynes using hydrobromic and hydrochloric acids as halogenating agents, with the sole byproduct being hydrogen gas. This e‐halochalcogenation protocol generates electrophilic chalcogenium species under mild conditions in a simple, undivided cell setup, enabling the synthesis of 25 examples of chloro‐ and bromovinyl selenides and sulfides with yields ranging from 10 % to 94 %, predominantly as the E‐isomer. The synthetic utility of the halovinyl chalcogenides was demonstrated through various transformations, yielding densely functionalized tetra‐substituted olefins. This underscores the versatility and efficiency of our method in assembling intricate molecular frameworks. Stereoselective electrochemical synthesis of E‐halovinyl chalcogenides and hydrogen gas from alkynes and dichalcogenides, such as diselenides or disulfides, in an undivided cell, utilizing HCl or HBr as halogenating agents. This e‐chalcogenation protocol generates electrophilic chalcogenyl halide species, which can be employed in other selenation coupling reactions.