Login / Signup

Fluoromethyl-2,4,6-trinitrophenylsulfonate: A New Electrophilic Monofluoromethylating Reagent.

Marco ReichelSami SileAndreas KornathKonstantin Karaghiosoff
Published in: The Journal of organic chemistry (2021)
Fluoromethyl-2,4,6-trinitrophenylsulfonate has been prepared for the first time and qualified as a simple to use monofluoromethylating reagent. Its molecular structure in the solid state has been determined by single-crystal X-ray diffraction studies. This reagent proves to be effective for the electrophilic introduction of a CH2F group into selected chalcogen and nitrogen nucleophiles. Monofluoromethyl derivatives of various bifunctional N,O-nucleophiles have been synthesized using fluoromethyl-2,4,6-trinitrophenylsulfonate. Due to the good crystallizing properties of the anion, the fluoromethylated products as well as side products that are difficult to identify by nuclear magnetic resonance spectroscopy can readily be characterized by X-ray crystallographic techniques.
Keyphrases
  • solid state
  • high resolution
  • dual energy
  • electron microscopy
  • ionic liquid
  • computed tomography
  • room temperature
  • single molecule
  • mass spectrometry
  • highly efficient
  • contrast enhanced