Visible-light-initiated tandem synthesis of difluoromethylated oxindoles in 2-MeTHF under additive-, metal catalyst-, external photosensitizer-free and mild conditions
An efficient and eco-friendly protocol for synthesizing difluoromethylated oxindoles through a visible-light-induced one-pot tandem reaction of N-arylacrylamides, difluoroacetic acid and PhI(OAc)2 was developed. This reaction proceeded in the absence of any additive, base, metal-catalyst and externa...
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Published in | Chinese chemical letters Vol. 32; no. 6; pp. 1907 - 1910 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
NEW YORK
Elsevier B.V
01.06.2021
Elsevier College of Chemistry and Materials Science,Hunan Agricultural University,Changsha 410128,China%School of Chemistry and Chemical Engineering,University of South China,Hengyang 421001,China%Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation,Changsha University of Science and Technology,Changsha 410114,China |
Subjects | |
Online Access | Get full text |
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Summary: | An efficient and eco-friendly protocol for synthesizing difluoromethylated oxindoles through a visible-light-induced one-pot tandem reaction of N-arylacrylamides, difluoroacetic acid and PhI(OAc)2 was developed. This reaction proceeded in the absence of any additive, base, metal-catalyst and external photosensitizer, using cheap CHF2CO2H as a difluoromethylation reagent and bulk biomass-derived 2-MeTHF as a solvent.
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An efficient and eco-friendly protocol for synthesizing difluoromethylated oxindoles through a visible-light induced one-pot tandem reaction of N-arylacrylamides, difluoroacetic acid and PhI(OAc)2 was developed. This reaction proceeded in the absence of any additive, base, metal-catalyst and external photosensitizer, using cheap and easily available CHF2CO2H as the difluoromethylation reagent and bulk biomass-derived 2-MeTHF as the sole solvent. 26 Examples of N-arylacrylamide substrates were investigated, and all of them successfully underwent difluoromethylation to deliver the target products in good to excellent yields. |
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ISSN: | 1001-8417 1878-5964 |
DOI: | 10.1016/j.cclet.2021.01.021 |