4.5 Article

Electrolyte-Triggered C5-Selective Trifluoromethylation and Halogenation of 8-Aminoquinoline Derivatives

Journal

ASIAN JOURNAL OF ORGANIC CHEMISTRY
Volume 10, Issue 3, Pages 559-562

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ajoc.202000650

Keywords

electrolytes; trifluoromethylation; halogenation; 8-aminoquinolines; electrocatalysis

Funding

  1. National Natural Science Foundation of China, NSFC [21978273, 21576239]
  2. National Key R&D Program of China [2018YFC0214100]

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An efficient electrolyte-triggered trifluoromethylation and halogenation at C5 position of 8-aminoquinoline derivatives was developed, giving moderate to excellent yields of C-H functionalization products. The mild and green reactions had lower energy consumption and shorter reaction times, while avoiding the use of transition-metal catalysts and oxidants.
An efficient electrolyte-triggered trifluoromethylation and halogenation at C5 position of 8-aminoquinoline derivatives was developed, affording the C-H functionalization products in moderate to excellent yields. Furthermore, the mild and green reactions had lower energy consumption and shorter times. Most importantly, both transition-metal catalysts and oxidants were avoided.

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