ipso-Fluorination of aryltrimethylsilanes using xenon difluoride

Add time:08/03/2019    Source:sciencedirect.com

Reaction of aryltrimethylsilanes with xenon difluoride in C6F6/Pyrex® at room temperature gives aryl fluorides in good yield. The reaction is inhibited when acetonitrile is used as solvent but proceeds well in CFCl3/Pyrex® or CH2Cl2/Pyrex®. Pyrex® appears to be a very effective heterogeneous catalyst for this ipso-fluorination. The reaction does not proceed in PTFE, quartz, soda glass or glassy-carbon flasks or Pyrex® flasks pre-rinsed with 2 M NaOH. Aryltrimethylstannanes and arylboronic acids and their esters do not undergo ipso-fluorination under similar conditions. Plausible mechanisms involving electrophilic addition of polarised xenon difluoride [FXeδ+⋯F→Pyrexδ−] followed by ligand coupling are discussed.

We also recommend Trading Suppliers and Manufacturers of PALLADIUM DIFLUORIDE (cas 13444-96-7). Pls Click Website Link as below: cas 13444-96-7 suppliers

Prev:A detailed spectrophotometric investigation of the complexation of palladium(II) with chloride and bromide
Next:Transferrin-conjugated pH-sensitive platform for effective delivery of porous palladium nanoparticles and paclitaxel in cancer treatment)