Issue 37, 2023

In situ generation of acyloxyphosphoniums for mild and efficient synthesis of thioesters

Abstract

We present a novel approach for in situ generation of acyloxyphosphoniums by premixing iodobenzene dicarboxylates and triphenylphosphine, resulting in efficient thioester synthesis (up to 100% yield). Stable solid iodobenzene dicarboxylates, achieved via carboxylate exchange, serve as hypervalent iodine precursors. The resulting acyloxyphosphoniums allow convenient one-pot thioester synthesis under mild conditions. Our method demonstrates facile acyloxyphosphonium production from iodobenzene dicarboxylates and Ph3P, enabling diverse thioester preparation. ESI-MS analysis confirms acyloxyphosphonium ion formation, pivotal in acylation. This strategy holds potential for combinatorial thioester synthesis and broader nucleophile modification applications.

Graphical abstract: In situ generation of acyloxyphosphoniums for mild and efficient synthesis of thioesters

Supplementary files

Article information

Article type
Communication
Submitted
17 Aug 2023
Accepted
04 Sep 2023
First published
06 Sep 2023

Org. Biomol. Chem., 2023,21, 7541-7545

In situ generation of acyloxyphosphoniums for mild and efficient synthesis of thioesters

T. Chai, X. Chiou, N. Lin, Y. Kuo and C. Lin, Org. Biomol. Chem., 2023, 21, 7541 DOI: 10.1039/D3OB01318A

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