# Ligand-free reductive amination via Pd-coated mechanocatalysis

**Authors:** Maximilian Wohlgemuth, Sarah Schmidt, Lars Beißel, Lars Borchardt

PMC · DOI: 10.1039/d5cc04707b · 2025-10-23

## TL;DR

A new method for reductive amination uses mechanical milling with palladium to produce amines efficiently without needing a ligand.

## Contribution

A sequential two-frequency milling protocol enables ligand-free reductive amination with high amine yields.

## Key findings

- A sequential two-frequency milling protocol separates imine formation and hydrogenation.
- Hydrophobic additives enhance reaction efficiency by excluding water.
- The method achieves up to 88% amine yields and works with various substrates.

## Abstract

Reductive amination under direct mechanocatalysis was enabled by a sequential two-frequency milling protocol, separating imine formation and hydrogenation. Strongly hydrophobic liquid additives accelerated the reaction by enhancing water exclusion. This approach allowed amine yields of up to 88% and was applicable to various aldehydes, ketones, and primary or secondary amines.

Reductive amination under direct mechanocatalysis was enabled by a sequential two-frequency milling protocol, separating imine formation and hydrogenation.

## Linked entities

- **Chemicals:** palladium (PubChem CID 23938), aldehydes (PubChem CID 6449839)

## Full-text entities

- **Chemicals:** water (MESH:D014867), aldehydes (MESH:D000447), Pd (MESH:D010165), ketones (MESH:D007659), primary (-), imine (MESH:D007097), amine (MESH:D000588)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12581175/full.md

---
Source: https://tomesphere.com/paper/PMC12581175