4.7 Article

Reactivity of a Hypervalent Iodine Trifluoromethylating Reagent toward THF: Ring Opening and Formation of Trifluoromethyl Ethers

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JOURNAL OF ORGANIC CHEMISTRY
卷 75, 期 5, 页码 1779-1782

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AMER CHEMICAL SOC
DOI: 10.1021/jo9025429

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  1. ETH Zurich

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1-Trifluoromethyl-1,2-benziodoxol-3-(1H)-one (1) is able to transfer the electrophilic CF3 group to the oxygen atom of THF in the presence of a Lewis or Bronsted acid. This results in a new ring-opening reaction of THF yielding trifluoromethyl ethers. Details of this reaction and the insight gained into the mechanism of action of reagent 1 are reported.

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