Organophotochemical SNAr Reactions of Mildly Electron‐Poor Fluoroarenes

C–F functionalization of arenes with a range of alcohol and pyrazole nucleophiles has been achieved without the need for metal catalysts or highly electron‐poor substrates. Treatment of fluoroarenes with alcohols or pyrazoles and DDQ under irradiation by blue LED light provides the corresponding sub...

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Veröffentlicht in:European journal of organic chemistry 2020-05, Vol.2020 (18), p.2766-2770
Hauptverfasser: Sheridan, Thomas, Yayla, Hatice G., Lian, Yajing, Genovino, Julien, Monck, Nat, Burton, Jonathan W.
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Sprache:eng
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Zusammenfassung:C–F functionalization of arenes with a range of alcohol and pyrazole nucleophiles has been achieved without the need for metal catalysts or highly electron‐poor substrates. Treatment of fluoroarenes with alcohols or pyrazoles and DDQ under irradiation by blue LED light provides the corresponding substituted products. The procedure is complementary to classical SNAr chemistry which generally requires basic reaction conditions and high temperatures, and provides products under non‐basic conditions at ≈ 40 °C. C–F functionalization of arenes with a range of alcohol and pyrazole nucleophiles has been achieved without the need for metal catalysts or highly electron‐poor substrates. Treatment of fluoroarenes with alcohols or pyrazoles and DDQ under irradiation by blue LED light provides the corresponding substituted products.
ISSN:1434-193X
1099-0690
DOI:10.1002/ejoc.202000337