Answers are grounded in this paper and cite their sources.
Methoxybenzenes and ‐naphthalenes are benzotriazolylmethylated in the para‐position or if this is blocked in an ortho‐ position. The methylene groups in the products are readily substituted by electrophiles via the lithiated derivatives. Displacement of the benzotriazole group can be effected by organometallic reagents or by electron‐rich benzoid compounds to afford a versatile method for the synthesis of substituted aryl ethers.
No takes yet. Share an insight, caveat, or question.
Katritzky et al. (1991) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: