Dehydrogenative transformation of alcoholic substrates in aqueous media catalyzed by an iridium complex having a functional ligand with α-Hydroxypyridine and 4,5-Dihydro-1H-imidazol-2-yl Moieties

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Abstract

A new catalytic system that employs water as an environmentally friendly solvent for the dehydrogenative oxidation of alcohols and lactonization of diols has been developed. In this catalytic system, a water-soluble dicationic iridium complex having a functional ligand that comprises α-hydroxypyridine and 4,5-dihydro-1H-imidazol-2-yl moieties exhibits high catalytic performance. For example, the catalytic dehydrogenative oxidation of 1-phenylethanol in the presence of 0.25 mol % of the iridium catalyst and base under reflux in water proceeded to give acetophenone in 92% yield. Additionally, under similar reaction conditions, the iridium-catalyzed dehydrogenative lactonization of 1,2-benzenedimethanol gave phthalide in 98% yield.

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Yoshida, M., Wang, H., Shimbayashi, T., & Fujita, K. I. (2018). Dehydrogenative transformation of alcoholic substrates in aqueous media catalyzed by an iridium complex having a functional ligand with α-Hydroxypyridine and 4,5-Dihydro-1H-imidazol-2-yl Moieties. Catalysts, 8(8). https://doi.org/10.3390/catal8080312

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