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. 2015 Jun 5;17(11):2652-5.
doi: 10.1021/acs.orglett.5b01024. Epub 2015 May 12.

Palladium-catalyzed C-H ethoxycarbonyldifluoromethylation of electron-rich heteroarenes

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Palladium-catalyzed C-H ethoxycarbonyldifluoromethylation of electron-rich heteroarenes

Changdong Shao et al. Org Lett. .

Abstract

The first Pd-catalyzed C-H ethoxycarbonyldifluoromethylation with BrCF2CO2Et has been developed. The use of a bidentate phosphine ligand (Xantphos) is critical for the reaction to occur. A variety of electron-rich heteroarenes, including indoles, furans, thiophenes, and pyrroles, can be ethoxycarbonyldifluoromethylated in moderate to excellent yields. The reactions take place at the C-H bonds adjacent to the heteroatoms with high regioselectivity. This method provides a new protocol for the introduction of difuoroalkyl groups into electron-rich heteroarenes.

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