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Automation and Microfluidics for the Efficient, Fast, and Focused Reaction Development of Asymmetric Hydrogenation Catalysis.
van Putten, Robbert; Eyke, Natalie S; Baumgartner, Lorenz M; Schultz, Victor L; Filonenko, Georgy A; Jensen, Klavs F; Pidko, Evgeny A.
Afiliação
  • van Putten R; Inorganic Systems Engineering, Department of Chemical Engineering, Delft University of Technology, Van der Maasweg 9, 2629HZ, Delft, Netherlands.
  • Eyke NS; Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, 02139, Cambridge, Massachusetts, United States.
  • Baumgartner LM; Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, 02139, Cambridge, Massachusetts, United States.
  • Schultz VL; Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, 02139, Cambridge, Massachusetts, United States.
  • Filonenko GA; Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, 02139, Cambridge, Massachusetts, United States.
  • Jensen KF; Inorganic Systems Engineering, Department of Chemical Engineering, Delft University of Technology, Van der Maasweg 9, 2629HZ, Delft, Netherlands.
  • Pidko EA; Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, 02139, Cambridge, Massachusetts, United States.
ChemSusChem ; 15(14): e202200333, 2022 Jul 21.
Article em En | MEDLINE | ID: mdl-35470567
ABSTRACT
Automation and microfluidic tools potentially enable efficient, fast, and focused reaction development of complex chemistries, while minimizing resource- and material consumption. The introduction of automation-assisted workflows will contribute to the more sustainable development and scale-up of new and improved catalytic technologies. Herein, the application of automation and microfluidics to the development of a complex asymmetric hydrogenation reaction is described. Screening and optimization experiments were performed using an automated microfluidic platform, which enabled a drastic reduction in the material consumption compared to conventional laboratory practices. A suitable catalytic system was identified from a library of RuII -diamino precatalysts. In situ precatalyst activation was studied with 1 H/31 P nuclear magnetic resonance (NMR), and the reaction was scaled up to multigram quantities in a batch autoclave. These reactions were monitored using an automated liquid-phase sampling system. Ultimately, in less than a week of total experimental time, multigram quantities of the target enantiopure alcohol product were provided by this automation-assisted approach.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Microfluídica / Álcoois Idioma: En Revista: ChemSusChem Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Microfluídica / Álcoois Idioma: En Revista: ChemSusChem Ano de publicação: 2022 Tipo de documento: Article