4.8 Article

Carboxylic Acid Deoxyfluorination and One-Pot Amide Bond Formation Using Pentafluoropyridine (PFP)

Journal

ORGANIC LETTERS
Volume 23, Issue 15, Pages 5793-5798

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.1c01953

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Funding

  1. Medical Research Council (MRC) Global Challenges Research Fund (GCRF) [MR/P027989/1A]
  2. Leverhulme Trust [ECF-2020-454]
  3. Leverhulme Trust Early Career Fellowship (Durham University)

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This work utilizes pentafluoropyridine (PFP) in the deoxyfluorination of carboxylic acids to acyl fluorides and in a one-pot amide bond formation. The method allows for high yields of amides to be readily obtained under mild conditions.
This work describes the application of pentafluoropyridine (PFP), a cheap commercially available reagent, in the deoxyfluorination of carboxylic acids to acyl fluorides. The acyl fluorides can be formed from a range of acids under mild conditions. We also demonstrate that PFP can be utilized in a one-pot amide bond formation via in situ generation of acyl fluorides. This one-pot deoxyfluorination amide bond-forming reaction gives ready access to amides in yields of <= 94%.

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