Direct Synthesis of 2-(4-Hydroxyphenoxy)benzamide Derivatives from 2-Aryloxybenzamide via PhIO-Mediated Oxidation Reaction
The 2-(4-hydroxyphenoxy)benzamide scaffold is frequently found in a variety of bioactive compounds, displaying a broad spectrum of properties, such as antibacterial and antitumor effects. In this study, we developed a new method for synthesizing 2-(4-hydroxyphenoxy)benzamide derivatives from 2-aryloxybenzamide via a PhIO-mediated oxidation reaction. The optimal reaction conditions were established as follows: TFA was used as the solvent, PhIO served as the oxidant with a substrate-to-oxidant ratio of 1:2, and the reaction was conducted at room temperature. This method, characterized by mild reaction conditions, broad applicability, and a metal-free nature, considerably improves the accessibility of 2-(4-hydroxyphenoxy)benzamide derivatives, which have been challenging to prepare using previously reported methods.
Authors
- Daowei Huang
- Zhenhua Shang (ORCID: https://orcid.org/0000-0001-8570-7096)
- Haoran Cheng (ORCID: https://orcid.org/0000-0002-9844-5168)
- D Jiao
Institutions
- Hebei University of Science and Technology (CN)
- Hebei Chemical and Pharmaceutical College (CN)
Publication Details
- Journal
- Molecules
- Published
- 2024-12-22
- DOI
- https://doi.org/10.3390/molecules29246048
- Citations
- 1
- Primary Topic
- Oxidative Organic Chemistry Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.25
Funders
- Natural Science Foundation of Hebei Province