Electron-Transfer-Induced Reductive Cleavage of Phthalans:  Reactivity and Synthetic Applications

Abstract

The behavior of phthalan (1a) was investigated under conditions of electron transfer from alkali metals in aprotic solvents. Reaction with lithium in the presence of a catalytic amount of naphthalene in THF led to the reductive cleavage of an arylmethyl carbon−oxygen bond, with formation of a stable dilithium compound. Trapping of this intermediate with several electrophiles (alkyl halides, carbonyl derivatives, CO2) was successful. The extension of this procedure to several substituted phthalans (1b−i) was investigated, and the regiochemistry as well as the synthetic usefulness of these reactions are discussed