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.

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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
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article

Development of Kilogram-Scale Electrochemical Ni-Catalyzed Cross Electrophile Coupling in Flow

Suqi Zhang, Luana Cardinale, Marcel Schreier, Gregory L. Beutner et al.
Organic Process Research & Development
Radical Photochemical Reactions
article

Development of Kilogram-Scale Electrochemical Ni-Catalyzed Cross Electrophile Coupling in Flow

Suqi Zhang, Luana Cardinale, Marcel Schreier, Gregory L. Beutner, Benjamin M. Cohen, Shannon S. Stahl, M. K. Kelly, Karrin V. Sackett
article en

Abstract

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.

Organic Process Research & Development
University of Wisconsin–Madison (US), Bristol-Myers Squibb (United States) (US), Université Bourgogne Franche-Comté (FR)
Industry, innovation and infrastructure
Openalex Percentile: Top 12%
Radical Photochemical Reactions
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