Synlett 2024; 35(18): 2117-2122
DOI: 10.1055/a-2294-4029
letter

A Facile Procedure for Halodecarboxylation of Hydroxyaromatic Carboxylic Acids

Authors

  • Zhenbei Zhang

    a   College of Chemistry and Chemical Engineering, Henan Institute of Science and Technology, Xinxiang, 453002, P. R. of China
    b   School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, P. R. of China
  • Wenhui Sun

    a   College of Chemistry and Chemical Engineering, Henan Institute of Science and Technology, Xinxiang, 453002, P. R. of China
  • Zhishan Cao

    c   College of Resources and Environment , Henan Institute of Science and Technology, Xinxiang, 453002, P. R. of China
  • Guisheng Zhang

    b   School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, P. R. of China
  • Olha Bakumenko

    d   Department of Plant Protection, Sumy National Agrarian University, Sumy, 40021, Ukraine
  • Feng Xue

    a   College of Chemistry and Chemical Engineering, Henan Institute of Science and Technology, Xinxiang, 453002, P. R. of China

This work was supported by the Key Scientific and Technological Project of Henan Province (Nos. 222102310117 and 222102320259) and by a Postdoctoral Research Grant of Henan Province (No. 19030076).


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Abstract

An efficient approach is reported for the direct halodecarboxylation of hydroxyaromatic acids by using a readily available N-halosuccinimide (halo = Cl, Br) as the sole promoter in ethanol at room temperature without any other catalyst or additive. This environmentally friendly route tolerates a wide substrate scope with good to excellent yields under convenient conditions.

Supporting Information



Publikationsverlauf

Eingereicht: 03. Januar 2024

Angenommen nach Revision: 25. März 2024

Accepted Manuscript online:
25. März 2024

Artikel online veröffentlicht:
23. April 2024

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