期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 137, 期 18, 页码 5916-5922出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.5b01745
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资金
- Israel Science Foundation [1073/10, 763/14]
- Bernice and Peter Cohn Catalysis Research Fund
- Helen and Martin Kimmel Center for Molecular Design
The synthesis of benzaldehyde. derivatives by oxygenation of methylarenes is of significant conceptual and practical interest because these compounds are important chemical intermediates whose synthesis is still carried out by nonsustainable methods with very low atom economy and formation of copious amounts of waste. Now an oxygenation reaction With a 100% theoretical atom economy using a polyoxometalate oxygen donor has beet). found: The product yield is typically above 95% with no overoxidation to benzoic acids; H-2 is released by electrolysis, enabling additional reaction cycles. An electrocatalytic cycle is also feasible. This reaction is possible through the use of an aqueous sulfuric acid solvent, in an aqueous biphasic reaction mode that also allows simple catalyst recycling and recovery. The solvent plays a key role in the reaction mechanism by protonating the polyoxometalate thereby enabling the activation of the methylarenes by an electron transfer process. After additional proton transfer and oxygen transfer steps, benzylic alcohols are formed that further react by an electron transfer proton, transfer sequence forming benzaldehyde derivatives.
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