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