Divergent Synthesis of 1,3,5-Trisubstituted Benzenes from 2,3,5-Triiodobenzoic acid

Abstract

Based on our previous explorations of o-diiodoarene/NaH as a novel aryne-generation system, herein we present an efficient route for divergent synthesis of 1,3,5-trisubstituted benzenes. Since carboxylic acid could be converted into a lot of functional groups, in this protocol, the readily available and inexpensive 2,3,5-triiodobenzoic acid (TIBA) was employed as the starting material for preparation of diverse aryne precursors. With this aryne-generation toolbox, a series of transformations were achieved between various nucleophiles and these aryne precursors, producing 5-iodo-1,3-disubstituted benzenes as valuable intermediates. The subsequent Ullmann reaction then gave hetero-1,3,5-trisubstituted benzenes.

Supplementary files

Article information

Article type
Communication
Submitted
27 Apr 2025
Accepted
04 Jun 2025
First published
04 Jun 2025

Org. Biomol. Chem., 2025, Accepted Manuscript

Divergent Synthesis of 1,3,5-Trisubstituted Benzenes from 2,3,5-Triiodobenzoic acid

H. Lin, J. Qi, F. Luo, Z. Zhu, H. Zhu, Y. Ge, Y. Hu, W. Wang, S. Zhang and X. Chen, Org. Biomol. Chem., 2025, Accepted Manuscript , DOI: 10.1039/D5OB00568J

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