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Selective Hydrodeoxygenation of Esters to Unsymmetrical Ethers over a Zirconium Oxide-Supported Pt–Mo Catalyst

[Image: see text] The catalytic hydrodeoxygenation (HDO) of carbonyl oxygen in esters using H(2) is an attractive method for synthesizing unsymmetrical ethers because water is theoretically the sole coproduct. Herein, we report a heterogeneous catalytic system for the selective HDO of esters to unsy...

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Detalles Bibliográficos
Autores principales: Sakoda, Katsumasa, Yamaguchi, Sho, Mitsudome, Takato, Mizugaki, Tomoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965830/
https://www.ncbi.nlm.nih.gov/pubmed/35373194
http://dx.doi.org/10.1021/jacsau.1c00535
Descripción
Sumario:[Image: see text] The catalytic hydrodeoxygenation (HDO) of carbonyl oxygen in esters using H(2) is an attractive method for synthesizing unsymmetrical ethers because water is theoretically the sole coproduct. Herein, we report a heterogeneous catalytic system for the selective HDO of esters to unsymmetrical ethers over a zirconium oxide-supported platinum–molybdenum catalyst (Pt–Mo/ZrO(2)). A wide range of esters were transformed into the corresponding unsymmetrical ethers under mild reaction conditions (0.5 MPa H(2) at 100 °C). The Pt–Mo/ZrO(2) catalyst was also successfully applied to the conversion of a biomass-derived triglyceride into the corresponding triether. Physicochemical characterization and control experiments revealed that cooperative catalysis between Pt nanoparticles and neighboring molybdenum oxide species on the ZrO(2) surface plays a key role in the highly selective HDO of esters. This Pt–Mo/ZrO(2) catalyst system offers a highly efficient strategy for synthesizing unsymmetrical ethers and broadens the scope of sustainable reaction processes.