Continuous Preparationof Trifluoromethyl Diazomethanein Flow Using In-Line Membrane Phase SeparationApplicationto the Catalytic Asymmetric Cyclopropanation of Substituted Styrenes

Trifluoromethyl diazomethane (TFDM) is a versatile reagent in organic synthesis and medicinal chemistry efforts. The utility of TFDM is hampered by safety concerns on scale. A novel method for the generation of dry, acid-free concentrated solutions of TFDM in a flow is reported here. The inclusion of an in-line liquid–liquid phase separator was a critical component in the flow scheme. The resulting dry stream could be coupled to a reactor containing a chiral ruthenium catalyst and styrene substrate to enantioselectively construct <i>trans</i>-trifluoromethyl-substituted cyclopropanes in a plug flow reactor–batch train. This system was utilized to access a variety of enantioenriched <i>trans</i>-trifluoromethyl-substituted cyclopropanes.

Publication Details

Journal
Figshare
Published
2025-03-04
DOI
https://doi.org/10.1021/acs.oprd.4c00477.s001
Primary Topic
Innovative Microfluidic and Catalytic Techniques Innovation
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article
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Continuous Preparationof Trifluoromethyl Diazomethanein Flow Using In-Line Membrane Phase SeparationApplicationto the Catalytic Asymmetric Cyclopropanation of Substituted Styrenes

Figshare
Innovative Microfluidic and Catalytic Techniques Innovation
article

Continuous Preparationof Trifluoromethyl Diazomethanein Flow Using In-Line Membrane Phase SeparationApplicationto the Catalytic Asymmetric Cyclopropanation of Substituted Styrenes

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Abstract

Trifluoromethyl diazomethane (TFDM) is a versatile reagent in organic synthesis and medicinal chemistry efforts. The utility of TFDM is hampered by safety concerns on scale. A novel method for the generation of dry, acid-free concentrated solutions of TFDM in a flow is reported here. The inclusion of an in-line liquid–liquid phase separator was a critical component in the flow scheme. The resulting dry stream could be coupled to a reactor containing a chiral ruthenium catalyst and styrene substrate to enantioselectively construct <i>trans</i>-trifluoromethyl-substituted cyclopropanes in a plug flow reactor–batch train. This system was utilized to access a variety of enantioenriched <i>trans</i>-trifluoromethyl-substituted cyclopropanes.

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Innovative Microfluidic and Catalytic Techniques Innovation
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