An electrosynthesis of 1,3,4-oxadiazoles from N-acyl hydrazones

Luke Chen, James D. F. Thompson*, Craig Jamieson*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

The 1,3,4-oxadiazole is a widely encountered motif in the areas of pharmaceuticals, materials, and agrochemicals. This work has established a mediated electrochemical synthesis of 2,5-disubstituted 1,3,4-oxadiazoles from N-acyl hydrazones. Using DABCO as the optimal redox mediator has enabled a mild oxidative cyclisation, without recourse to stoichiometric oxidants. In contrast to previous methods, this indirect electrochemical oxidation has enabled a broad range of substrates to be accessed, with yields of up to 83 %, and on gram scale. The simplicity of the method has been further demonstrated by the development of a one-pot procedure, directly transforming readily available aldehydes and hydrazides into valuable heterocycles.
Original languageEnglish
Number of pages10
JournalChemistry - A European Journal
Early online date18 Sept 2024
DOIs
Publication statusE-pub ahead of print - 18 Sept 2024

Keywords

  • 1,3,4-oxadiazoles
  • electrochemistry
  • hydrazones
  • indirect electrolysis
  • oxidation

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