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

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.

Publication Details

Journal
Strathprints: The University of Strathclyde institutional repository (University of Strathclyde)
Published
2024-12-10
Primary Topic
Seismic Imaging and Inversion Techniques
Type
article
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article

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

Strathprints: The University of Strathclyde institutional repository (University of Strathclyde)
Seismic Imaging and Inversion Techniques
article

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

article en

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.

Strathprints: The University of Strathclyde institutional repository (University of Strathclyde)
Engineering and Physical Sciences Research Council
Openalex Percentile: Top 45%
Seismic Imaging and Inversion Techniques
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