The reaction of activated alcohols with the O-(tert-butyl) Se-phenyl selenocarbonate/hydroiodic acid system to give the corresponding alkyl phenyl selenides is described. The direct conversion of the hydroxyl group into a phenylselenenyl group is also extended to allyl- and tertiary alkyl alcohols. This work provides a safe, metal-free, and operationally simple process for the preparation of alkyl phenyl selenides from benzylic alcohols.

Metal-Free Synthesis of Alkyl Phenyl Selenides by Reaction of Activated Alcohols with the O-(tert-Butyl) Se-Phenyl Selenocarbonate/HI System

Siciliano C.
Membro del Collaboration Group
2021-01-01

Abstract

The reaction of activated alcohols with the O-(tert-butyl) Se-phenyl selenocarbonate/hydroiodic acid system to give the corresponding alkyl phenyl selenides is described. The direct conversion of the hydroxyl group into a phenylselenenyl group is also extended to allyl- and tertiary alkyl alcohols. This work provides a safe, metal-free, and operationally simple process for the preparation of alkyl phenyl selenides from benzylic alcohols.
2021
alcohol
benzeneselenol
hydroiodic acid
nucleophilic substitution
selenides
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11770/325553
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