Preparation and Spectral Properties of 2-(2, 4-Dichlorophenyl)-2-(1, 2, 3, 5-tetrazol-1-ylmethyl)-1, 3-dioxolan-4-ylmethanol and Its Benzoate and Methanesulfonate

Abstract

The title compounds were prepared by nucleophilic substitution by tetrazole anion of the corresponding bromide (1). followed by hydrolysis and methanesulfonylation. The site of alkylation of the tetrazole anion was determined by comparison of the ¹³C-nuclear magnetic resonance spectrum with those of N-methyltetrazoles.