Publication | Open Access
N‐Heterocyclic Carbene‐Catalyzed Oxidative Esterification Reaction of Aldehydes with Alkyl Halides under Aerobic Conditions
43
Citations
62
References
2011
Year
Chemical EngineeringBreslow IntermediateEngineeringCross-coupling ReactionAerobic ConditionsAlkyl HalidesNatural SciencesDiversity-oriented SynthesisElectrosynthesisOxidative Esterification ReactionOrganic ChemistryCatalysisMolecular CatalysisChemistryCatalytic SynthesisGood Yields
Abstract An efficient N‐heterocyclic carbene‐catalyzed oxidative esterification reaction of aldehydes with alkyl halides or alkyl 4‐methylbenzenesulfonate is reported. It was worth noting that (1) the configuration of alkyl halides or alkyl 4‐methylbenzenesulfonates was inverted completely, and (2) the presence of oxygen was crucial for this transformation. The reaction proceeded smoothly under mild conditions and various esters were afforded in moderate to good yields. In addition, we have developed an efficient tandem oxidation/esterification reaction of alcohols. This methodology provides a rare example of a reaction of the Breslow intermediate to sp 3 ‐carbon centered electrophiles.
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