CuI-Catalyzed Pentafluoroethylation of Aryl Iodides in the Presence of Tetrafluoroethylene and Cesium Fluoride: Determining the Route to the Key Pentafluoroethyl CuI Intermediate

被引:39
作者
Ohashi, Masato [1 ]
Ishida, Naoyoshi [1 ]
Ando, Kota [1 ]
Hashimoto, Yu [1 ]
Shigaki, Anna [1 ]
Kikushima, Kotaro [1 ]
Ogoshi, Sensuke [1 ]
机构
[1] Osaka Univ, Dept Appl Chem, Fac Engn, Suita, Osaka 5650871, Japan
关键词
catalytic reaction; copper; fluorine; fluorocupration; pentafluoroethylation; TRIFLUOROMETHYLATION REACTIONS; MEDICINAL CHEMISTRY; ARYLBORONIC ACIDS; CONVENIENT METHOD; BOND ACTIVATION; COPPER REAGENT; COMPLEXES; DERIVATIVES; ALKYNES; BROMIDES;
D O I
10.1002/chem.201802415
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Cu(I)-catalyzed pentafluoroethylation of iodoarenes via the fluorocupration of tetrafluoroethylene (TFE) is disclosed. The active species, (phen)CuC2F5, was isolated and its molecular structure confirmed by a single-crystal X-ray diffraction analysis. The key to the successful suppression of the competing oligomerization of TFE is to refrain from stirring the reaction mixture. A mechanistic study clearly discarded the possibility that the catalytic reaction proceeds via a radical pathway.
引用
收藏
页码:9794 / 9798
页数:5
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