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Continuous Flow Chemistry: Reaction of Diphenyldiazomethane with p-Nitrobenzoic Acid
Published on: November 15, 2017
Safe and Facile Access to Nonstabilized Diazoalkanes Using Continuous Flow Technology
Pauline Rullière1, Guillaume Benoit1, Emmanuelle M D Allouche1
1Faculty of Arts and Sciences, Department of Chemistry, Université de Montreal, P.O. Box 6128 Station Downtown, Montreal, Quebec, H3C 3J7, Canada.
Abstract:
Despite the high synthetic potential of nonstabilized diazo compounds, their utilization has always been hampered by stability, toxicity, and safety issues. The present method opens up access to the most reactive nonstabilized diazoalkanes. Among diazo compounds, nonstabilized alkyl diazo compounds are the least represented because of their propensity to degrade during preparation. The continuous flow oxidation process of hydrazones on a silver oxide column afforded an output stream of base- and metal-free pure diazo solution in dichloromethane. Starting from innocuous ketones and aldehydes, this methodology allows the production of a broad range of unprecedented diazoalkanes compounds in excellent yields, while highlighting their synthetic potential and the possibility of safe large-scale diazo production.
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