Cobalt-Catalysed Reductive Etherification Using Phosphine Oxide Promoters under Hydroformylation Conditions

A phosphine-oxide-promoted, cobalt-catalysed reductive etherification using syngas as a reductant is reported. This novel methodology was successfully used to prepare a broad range of unsymmetrical ethers from various aldehydes and alcohols containing diverse functional groups, and was scaled-up to multigram scale under comparably mild conditions. Mechanistic experiments support an acetalization-hydrogenation sequence.

Automated summary

A phosphine-oxide-promoted, cobalt-catalysed reductive etherification using syngas as a reductant has been reported in this study. This novel methodology has been successfully applied to prepare unsymmetrical ethers from a wide range of aldehydes and alcohols containing diverse functional groups, and the reaction has been scaled-up to multigram scale under relatively mild conditions. Mechanistic experiments suggest an acetalization-hydrogenation sequence.