March 26, 2018
Journal Article

Palladium-Catalyzed Reductive Insertion of Alcohols into Aryl Ether Bonds

Abstract

Pd/C catalyzes C-O bond cleavage of aryl ethers (diphenyl ether and cyclohexyl phenyl ether) by methanol in H2. The aromatic C-O bond is cleaved by reductive methanolysis, which is initiated by Pd-catalyzed partial hydrogenation of one phenyl ring to form an enol ether. The enol ether reacts rapidly with methanol to form a ketal, which generates methoxycyclohexene by eliminating phenol or an alkanol. Subsequent hydrogenation leads to methoxycyclohexane.

Revised: February 11, 2020 | Published: March 26, 2018

Citation

Wang M., O.Y. Gutierrez-Tinoco, D.M. Camaioni, and J.A. Lercher. 2018. Palladium-Catalyzed Reductive Insertion of Alcohols into Aryl Ether Bonds. Angewandte Chemie International Edition 130, no. 14:3809-3813. PNNL-SA-129112. doi:10.1002/ange.201709445