Site‐Fixed Hydroboration of Terminal and Internal Alkenes using BX₃/^<i>i</i>Pr₂NEt**

Abstract

An unprecedented and general hydroboration of alkenes with BX₃ (X=Br, Cl) as the boration reagent in the presence of ⁱ Pr₂ NEt is reported. The addition of ⁱ Pr₂ NEt not only suppresses alkene polymerization and haloboration side reactions but also provides an "H" source for hydroboration. More importantly, the site-fixed installation of a boryl group at the original position of the internal double bond is readily achieved in contrast to conventional transition-metal-catalyzed hydroboration processes. Further application to the synthesis of 1,n-diborylalkanes (n=3-10) is also demonstrated. Preliminary mechanistic studies reveal a major reaction pathway that involves radical species and operates through a frustrated Lewis pair type single-electron-transfer mechanism.