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| - Mechanism of Homogeneous Iridium-Catalyzed Alkylation of Amines with Alcohols from a DFT Study
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| Abstract
| - A DFT study on the {IrCp*}-catalyzed N-alkylation of amines by alcohols showed that the two hydrogen atoms eliminated from the alcohol and added to the imine are tranferred as H− and H+, the hydride going to and from the metal and the proton to and from the carbonate base. The rate of the reaction increases with lower basicity of the amine substrate.
- The reaction mechanism for the Ir-catalyzed alkylation of primary amines with primary alcohols has been studied by DFT calculations. The three-step reaction pathway consists of Ir-catalyzed alcohol dehydrogenation to aldehyde, amine-aldehyde condensation to imine, and then Ir-catalyzed imine hydrogenation to amine. The presence of two essentially mirror-image reactions (dehydrogenation of the alcohol and hydrogenation of the imine) makes the reaction intrinsically challenging. The reaction is however shown to favor the product-forming direction because the dehydrogenation of an alcohol via β-H elimination has a lower barrier than the dehydrogenation of an amine. The prediction that amine dissociation is rate determining is consistent with the faster rate experimentally found here for the weakly basic amine TsNH2. The ancillary carbonate ligand on Ir is shown to be involved in the hydrogen transfer. The two hydrogen atoms eliminated from the alcohol and added to the imine are transferred as H− and H+, the hydride going to and from the metal and the proton to and from the carbonate base.
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| - Homogeneous Ir-Catalyzed Alkylation of Amines with Alcohols
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