4.8 Article

Fast continuous alcohol amination employing a hydrogen borrowing protocol

Journal

GREEN CHEMISTRY
Volume 21, Issue 1, Pages 59-63

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8gc03328e

Keywords

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Funding

  1. EPSRC [EP/K009494/1, EP/M004120/1, EP/K039520/1]
  2. Eli Lilly & Co. through the Lilly Research Award Program (LRAP)
  3. Eli Lilly Co.
  4. EPSRC [EP/K009494/1, EP/K039520/1, EP/M004120/1] Funding Source: UKRI

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A continuous flow method for the direct conversion of alcohols to amines via a hydrogen borrowing approach is reported. The method utilises a low loading (0.5%) of a commercial catalyst system ([Ru(p-cymene)Cl-2](2) and DPEPhos), reagent grade solvent and is selective for primary alcohols. Successful methylation of amines using methanol and the direct dimethylamination of alcohols using commercial dimethylamine solution are reported. The synthesis of two pharmaceutical agents Piribedil (5) and Buspirone (25) were accomplished in good yields employing these new methods.

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