4.8 Article

Deoxyfluorination of Electron-Deficient Phenols

Journal

ORGANIC LETTERS
Volume 25, Issue 20, Pages 3649-3653

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.3c01018

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In this study, a simple method for the synthesis of 2-chloro-1,3-bis-(2,6-diisopropylphenyl)-imidazolium salts in aqueous media using hypochlorite as a chlorinating agent was reported. Additionally, an air-stable and moisture-insensitive deoxyfluorination reagent based on poly-[hydrogen fluoride] salt was presented, which can convert electron-deficient phenols or aryl silyl ethers into corresponding aryl fluorides in the presence of DBU as a base, with high yields and good tolerance to functional groups.
In this study, wereport a facile synthesis of 2-chloro-1,3-bis-(2,6-diisopropylphenyl)-imidazoliumsalts in aqueous media under ambient conditions using hypochloriteas a chlorinating agent. In addition, an air-stable and moisture-insensitivedeoxyfluorination reagent based on poly-[hydrogen fluoride] salt ispresented, which is capable of converting electron-deficient phenolsor aryl silyl ethers into the corresponding aryl fluorides in thepresence of DBU as a base, with good to excellent yields and hightolerance to functional groups.

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