One-pot synthesis of xanthones from 2-nitrobenzyl alcohol and phenol catalyzed by Cu(OTf) <sub>2</sub> -1,10-phenanthroline

In this paper, we present an efficient and straightforward one-pot synthesis of xanthones in high yield (88%). The reaction employs a Cu(OTf)<sub>2</sub>-1,10-phenanthroline complex as the catalyst and 2-nitrobenzyl alcohol and phenol as the substrates. The reaction proceeds under mild conditions, providing a convenient approach for the formation of xanthones, which are valuable compounds in medicinal chemistry and materials science. This work not only broadens the synthetic scope of xanthones but also highlights the feasibility of carrying out substitution reactions of nitro groups on aromatic hydrocarbons.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00648a
Citations
1
Primary Topic
Synthesis of Indole Derivatives
Type
article
Field-Weighted Citation Impact
0.94

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article

One-pot synthesis of xanthones from 2-nitrobenzyl alcohol and phenol catalyzed by Cu(OTf) 2 -1,10-phenanthroline

Qing-Dong Liu, Xiaoning Feng, Yan Zhou, Bingbing Pan et al.
1 citations
Organic & Biomolecular Chemistry
Synthesis of Indole Derivatives
0.94
article

One-pot synthesis of xanthones from 2-nitrobenzyl alcohol and phenol catalyzed by Cu(OTf) 2 -1,10-phenanthroline

Qing-Dong Liu, Xiaoning Feng, Yan Zhou, Bingbing Pan, Gengxiu Zheng, Lingfeng Gao, Xu Sun, Wei Long, Zheng Zhang
article en
1 citations

Abstract

In this paper, we present an efficient and straightforward one-pot synthesis of xanthones in high yield (88%). The reaction employs a Cu(OTf)<sub>2</sub>-1,10-phenanthroline complex as the catalyst and 2-nitrobenzyl alcohol and phenol as the substrates. The reaction proceeds under mild conditions, providing a convenient approach for the formation of xanthones, which are valuable compounds in medicinal chemistry and materials science. This work not only broadens the synthetic scope of xanthones but also highlights the feasibility of carrying out substitution reactions of nitro groups on aromatic hydrocarbons.

Organic & Biomolecular ChemistryVol. 23(26)
University of Jinan (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 25%
Synthesis of Indole Derivatives
0.94
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