Iron-catalysed hydroboration of non-activated imines and nitriles: Kinetic and mechanistic studies

Adineh Rezaei Bazkiaei, Michael Wiseman, Michael Findlater

Research output: Contribution to journalArticlepeer-review

Abstract

Iron-catalysed hydroboration of imines and nitriles has been developed under low catalyst loading (1 mol%) in the presence of HBpin. A wide scope of substrate was found to smoothly undergo hydroboration, including electron releasing/withdrawing and halogen substitution patterns and cyclic substrates which all afforded the corresponding amines in good to excellent yields. Dihydroboration of nitriles was achieved conveniently under solvent free and additive free conditions. Promisingly, this catalytic system is also capable of the hydroboration of challenging ketimine substrates. Preliminary kinetic analysis of imine hydroboration reveals a first-order dependence on catalyst concentration. Both HBpin and 4-fluorophenyl-N-phenylmethanimine (1b) appear to exhibit saturation kinetics with first order dependence up to 0.5 mmol HBpin and 0.75 mmol imine, respectively. Temperature-dependent rate experiments for imine hydroboration have also been explored. Activation parameters for the hydroboration of FPhCNPh (1b) were determined from the Eyring and Arrhenius plots with ΔS≠, ΔH≠, and Ea values of -28.69 (±0.3) e.u., 12.95 (±0.04) kcal mol-1, and 15.22 (±0.09) kcal mol-1, respectively. This journal is

Original languageEnglish
Pages (from-to)15284-15289
Number of pages6
JournalRSC Advances
Volume11
Issue number25
DOIs
StatePublished - Apr 23 2021

Fingerprint

Dive into the research topics of 'Iron-catalysed hydroboration of non-activated imines and nitriles: Kinetic and mechanistic studies'. Together they form a unique fingerprint.

Cite this