Continuous Preparation of Trifluoromethyl Diazomethane in Flow Using In-Line Membrane Phase Separation─Application to 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 trans-trifluoromethyl-substituted cyclopropanes in a plug flow reactor–batch train. This system was utilized to access a variety of enantioenriched trans-trifluoromethyl-substituted cyclopropanes.

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Publication Details

Journal
Organic Process Research & Development
Published
2025-03-04
DOI
https://doi.org/10.1021/acs.oprd.4c00477
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.79
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Continuous Preparation of Trifluoromethyl Diazomethane in Flow Using In-Line Membrane Phase Separation─Application to the Catalytic Asymmetric Cyclopropanation of Substituted Styrenes

Matthew G. Beaver, Kevin Crossley, Oleg L. Epstein, David Bauer et al.
1 citations
Organic Process Research & Development
Fluorine in Organic Chemistry
0.79
article

Continuous Preparation of Trifluoromethyl Diazomethane in Flow Using In-Line Membrane Phase Separation─Application to the Catalytic Asymmetric Cyclopropanation of Substituted Styrenes

Matthew G. Beaver, Kevin Crossley, Oleg L. Epstein, David Bauer, Tyler K. Allred, Olga A. Мukhina, Michael Frohn, James I. Murray, Jie Yan
article en
1 citations

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 trans-trifluoromethyl-substituted cyclopropanes in a plug flow reactor–batch train. This system was utilized to access a variety of enantioenriched trans-trifluoromethyl-substituted cyclopropanes.

Organic Process Research & DevelopmentVol. 29(3)
Amgen (United States) (US), Pivotal (Canada) (CA), Université Bourgogne Franche-Comté (FR)
Clean water and sanitation
Openalex Percentile: Top 30%
Fluorine in Organic Chemistry
0.79
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