Development of Kilogram-Scale Electrochemical Ni-Catalyzed Cross Electrophile Coupling in Flow
High Resolution Image Download MS PowerPoint Slide Organic electrosynthesis opens novel routes for pharmaceutical production; however, limited knowledge and experience with the scale up of this technique have hindered its industrial implementation. In this work, we report a kilogram-scale flow electrochemical Ni-catalyzed cross-electrophile coupling (XEC) to prepare a key intermediate in the synthesis of the toll-like receptor (TLR) 7/8 inhibitor afimetoran. We successfully demonstrate scalability across 2 orders of magnitude while maintaining reaction performance. We also conduct a continuous 120 h reaction, highlighting compatibility with industrially relevant time scales. Key design aspects of our custom parallel-plate reactor are discussed that enabled kilogram-scale synthesis with a single electrode stack. This report showcases that with proper reaction engineering, electrochemical Ni-catalyzed XEC is a viable alternative to existing Pd-catalyzed cross-coupling methods.
Authors
- Suqi Zhang (ORCID: https://orcid.org/0000-0003-1196-4123)
- Luana Cardinale (ORCID: https://orcid.org/0000-0001-9867-3593)
- Marcel Schreier (ORCID: https://orcid.org/0000-0002-3674-5667)
- Gregory L. Beutner (ORCID: https://orcid.org/0000-0001-8779-1404)
- Benjamin M. Cohen (ORCID: https://orcid.org/0000-0002-7000-9292)
- Shannon S. Stahl (ORCID: https://orcid.org/0000-0002-9000-7665)
- M. K. Kelly (ORCID: https://orcid.org/0009-0003-5160-1041)
- Karrin V. Sackett
Institutions
- University of Wisconsin–Madison (US)
- Bristol-Myers Squibb (United States) (US)
- Université Bourgogne Franche-Comté (FR)
Publication Details
- Journal
- Organic Process Research & Development
- Published
- 2026-06-16
- DOI
- https://doi.org/10.1021/acs.oprd.6c00110
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00