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Radical Hydrodehalogenation of Aryl Bromides and Chlorides with Sodium Hydride and 1,4-Dioxane.

Tobias HokampAbhishek DewanjiMaximilian LübbesmeyerChristian Mück-LichtenfeldErnst-Ulrich WürthweinArmido Studer
Published in: Angewandte Chemie (International ed. in English) (2017)
A practical method for radical chain reduction of various aryl bromides and chlorides is introduced. The thermal process uses NaH and 1,4-dioxane as reagents and 1,10-phenanthroline as an initiator. Hydrodehalogenation can be combined with typical cyclization reactions, proving the nature of the radical mechanism. These chain reactions proceed by electron catalysis. DFT calculations and mechanistic studies support the suggested mechanism.
Keyphrases
  • density functional theory
  • molecular dynamics
  • case control