Issue 21, 2022, Issue in Progress

Palladium-catalysed difluoroolefination of benzyl tosylates toward the synthesis of gem-difluoro-2-trifluromethyl styrene derivatives

Abstract

We have presented an efficient method to access gem-difluoro-2-trifluromethyl styrene derivatives via palladium catalysis. This method features mild reaction conditions, broad substrate scope and good product yields. Moreover, gram–scale reactions demonstrated the robustness and potential of this method. Control experiments revealed that the –CF3 group was essential to the success of this transformation. Finally, the practicality of this method was successfully proven by three synthetic applications.

Graphical abstract: Palladium-catalysed difluoroolefination of benzyl tosylates toward the synthesis of gem-difluoro-2-trifluromethyl styrene derivatives

Supplementary files

Article information

Article type
Paper
Submitted
17 Apr 2022
Accepted
21 Apr 2022
First published
28 Apr 2022
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2022,12, 12983-12987

Palladium-catalysed difluoroolefination of benzyl tosylates toward the synthesis of gem-difluoro-2-trifluromethyl styrene derivatives

J. Xu, J. Liu, G. Chen, B. Xiong, X. Zhang and Z. Lian, RSC Adv., 2022, 12, 12983 DOI: 10.1039/D2RA02473J

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