Publication | Closed Access
Palladium-Catalyzed Coupling Reactions of Tetrafluoroethylene with Arylzinc Compounds
184
Citations
57
References
2011
Year
Chemical EngineeringCross-coupling ReactionEngineeringOrganofluorine CompoundsFluorous SynthesisPalladium-catalyzed Coupling ReactionsOrganic ChemistryOrganometallic CatalysisCatalysisChemistryCarbon-fluorine Bond ActivationChemical Industry
Organofluorine compounds are widely used in all aspects of the chemical industry. Although tetrafluoroethylene (TFE) is an example of an economical bulk organofluorine feedstock, the use of TFE is mostly limited to the production of poly(tetrafluoroethylene) and copolymers with other alkenes. Furthermore, no catalytic transformation of TFE that involves carbon-fluorine bond activation has been reported to date. We herein report the first example of a palladium-catalyzed coupling reaction of TFE with arylzinc reagents in the presence of lithium iodide, giving α,β,β-trifluorostyrene derivatives in excellent yields.
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