Related Experiment Video
Updated: Apr 25, 2026

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Triethylborane-initiated radical chain fluorination: a synthetic method derived from mechanistic insight
Cody Ross Pitts1, Bill Ling, Ryan Woltornist
1Department of Chemistry, Johns Hopkins University , 3400 North Charles Street, Baltimore, Maryland 21218, United States.
Abstract:
We offer a mild, metal-free sp(3) C-H fluorination alternative using Selectfluor and a substoichiometric amount of triethylborane--an established radical initiator in the presence of O2. This radical-chain-based synthetic method is particularly noteworthy as an offspring of the insight gained from a mechanistic study of copper-promoted aliphatic fluorination, constructively turning O2 from an enemy to an ally. Furthermore, BEt3/O2 is a preferred initiator in industrial processes, as it is economical, is low in toxicity, and lends way to easier workup.
Related Concept Videos
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
Radical Substitution: Allylic Bromination
Radical Chain-Growth Polymerization: Mechanism
Radical Chain-Growth Polymerization: Overview
Radical Substitution: Allylic Chlorination
Radical Chain-Growth Polymerization: Chain Branching

