C-F bond-cleavage reactions of fluoroalkanes with magnesium reagents and without metal catalysts

Org Lett. 2009 Apr 16;11(8):1765-8. doi: 10.1021/ol900208n.

Abstract

An unexpected C-F bond-cleavage reaction of unactivated fluoroalkanes with the well-known Grignard reagents without using metal catalysts has been discovered. For example, a reaction between 1-fluorooctane and phenyl magnesium chloride gave n-octylbenzene in moderate yield. This coupling reaction via the activation of an unactivated alkyl carbon-fluorine bond proceeds with phenylmagnesium chloride, whereas methylmagnesium chloride did not give the C-C cross-coupling product but rather a halogen exchange product.