Defluorosilylation of trifluoromethane: upgrading an environmentally damaging fluorocarbon
Daniel J. Sheldon, Greg Coates, Mark R. Crimmin
Abstract
. The reaction generates a bench stable fluorinated building block that shows promise as an easy-to-use difluoromethylating agent. The difluoromethyl group is an increasingly important bioisostere in active pharmaceutical ingredients, and therefore our methodology creates value from waste. The potential scalability of the process has been demonstrated by achieving the reaction on a gram-scale.
Topics & Concepts
FluorocarbonChemical engineeringEnvironmentally friendlyChemistryMaterials scienceOrganic chemistryEngineeringEcologyBiologyFluorine in Organic ChemistryInorganic Fluorides and Related CompoundsPer- and polyfluoroalkyl substances research