Green, Scalable, and Low-Cost Synthesis of Fluorine-Containing Bisphenol Monomers through a Synergistic Catalytic System

A facile, green, and scalable synthetic approach for the preparation of structurally diverse fluorine-containing bisphenols has been developed with trifluoroacetaldehyde hydrate that exhibits significant cost advantages. Compared with the conventional harsh conditions with hazardous reagents (using large amounts of anhydrous gaseous HCl/HF or methanesulfonic acid as the reaction medium), the developed method avoids these hazardous reagents and harsh conditions by exploiting the beneficial cooperation of a catalytic amount of TfOH and easily recyclable solvent HFIP, which readily allows hectogram-scale syntheses of fluorine-containing bisphenols. Further mechanistic studies revealed that the synergetic hydrogen bonding interactions between TfOH and HFIP play an important role in promoting this transformation efficiently with enhanced catalytic activity.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-11-11
DOI
https://doi.org/10.1021/acs.joc.5c02038
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
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article

Green, Scalable, and Low-Cost Synthesis of Fluorine-Containing Bisphenol Monomers through a Synergistic Catalytic System

Ziyan Wu, Feng Yun Yan, Chunman Jia, Guodong Fang et al.
The Journal of Organic Chemistry
Fluorine in Organic Chemistry
article

Green, Scalable, and Low-Cost Synthesis of Fluorine-Containing Bisphenol Monomers through a Synergistic Catalytic System

Ziyan Wu, Feng Yun Yan, Chunman Jia, Guodong Fang, Zhendong Zhao, Jinshan Li, Yuhao Wu, Xindi Li, Jialin Xie, Zhenchang Wen
article en

Abstract

A facile, green, and scalable synthetic approach for the preparation of structurally diverse fluorine-containing bisphenols has been developed with trifluoroacetaldehyde hydrate that exhibits significant cost advantages. Compared with the conventional harsh conditions with hazardous reagents (using large amounts of anhydrous gaseous HCl/HF or methanesulfonic acid as the reaction medium), the developed method avoids these hazardous reagents and harsh conditions by exploiting the beneficial cooperation of a catalytic amount of TfOH and easily recyclable solvent HFIP, which readily allows hectogram-scale syntheses of fluorine-containing bisphenols. Further mechanistic studies revealed that the synergetic hydrogen bonding interactions between TfOH and HFIP play an important role in promoting this transformation efficiently with enhanced catalytic activity.

The Journal of Organic ChemistryVol. 90(46)
Hainan University (CN), Hainan Provincial Hospital of Traditional Chinese Medicine (CN)
Openalex Percentile: Top 73%
Fluorine in Organic Chemistry
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