The reaction of o-trimethylsilylphenyllithium with carbonyl compounds
and subsequent halogenodesilylation with ICI afforded o-iodophenylcarb
inols in good yields, showing the usefulness of o-trimethylsilylphenhy
llithium as a synthetic equivalent of o-iodophenyl anion. The reaction
via a protected o-trimethylsilylphenylcarbinol is also shown.