The role of iodide promoters and the mechanism of ethylene carbonylation catalyzed by molybdenum hexacarbonyl

Abstract

In limited prior reports, molybdenum hexacarbonyl has been shown to be active in catalyzing ethylene carbonylation promoted by ethyl iodide. Here, we assess the productivity of this reaction with respect to various reaction parameters and provide an understanding of the mechanism by NMR and mass spectrometric studies of isotopically labeled reactants. 13C labeled reactants show that ethyl iodide promotes initiation but is not a participant in the primary catalytic cycle, in contrast to classical mechanisms for alcohol carbonylation with an iodide co-catalyst, such as in the Monsanto process. NMR spectroscopy shows incorporation of only one D from D2O into the carbon backbone of propionic acid products, and in a manner consistent with direct, reversible addition of ethylene to a Mo hydride intermediate. CO migratory insertion and a formal hydroxylation then yield propionic acid. Under the conditions described here, the overall cycle gives propionic acid in high selectivity and requiring low promoter loads.