4.8 Article

Rapid Ether and Alcohol C-O Bond Hydrogenolysis Catalyzed by Tandem High-Valent Metal Triflate plus Supported Pd Catalysts

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 136, 期 1, 页码 104-107

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AMER CHEMICAL SOC
DOI: 10.1021/ja411546r

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资金

  1. U.S. Department of Energy [DE-AC0206CH11357]
  2. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences
  3. NSF [CHE-1213235]
  4. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  5. Office of Science of the U.S. Department of Energy [DE-AC02-05CH11231]
  6. Direct For Mathematical & Physical Scien
  7. Division Of Chemistry [1213235] Funding Source: National Science Foundation

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The thermodynamically leveraged conversion of ethers and alcohols to saturated hydrocarbons is achieved efficiently with low loadings of homogeneous M(OTf)(n) + heterogeneous Pd tandem catalysts (M = transition metal; OTf = triflate; n = 4). For example, Hf(OTf)(4) mediates rapid endothermic ether reversible arrow alcohol and alcohol reversible arrow alkene equilibria, while Pd/C catalyzes the subsequent, exothermic alkene hydrogenation. The relative C-O cleavage rates scale as 30 degrees > 20 degrees > 1 degrees. The reaction scope extends to efficient conversion of biomass-derived ethers, such as THF derivatives, to the corresponding alkanes.

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