Synthesis of 3,4-Dihydro-2H-Pyrroles from Ketones,Aldehydes, and Nitro Alkanes via Hydrogenative Cyclization |
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Authors: | Barbara Klausfelder Patricia Blach Prof. Niels de Jonge Prof. Rhett Kempe |
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Affiliation: | 1. Anorganische Chemie II, Catalyst Design, Sustainable Chemistry Centre, University of Bayreuth, Universitätsstraße 30, 95440 Bayreuth, Germany;2. INM - Leibniz Institute for New Materials, Campus D2 2, 66123 Saarbrücken, Germany Department of Physics, Saarland University, Campus D2 2, 66123 Saarbrücken, Germany |
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Abstract: | Syntheses of N-heterocyclic compounds that permit a flexible introduction of various substitution patterns by using inexpensive and diversely available starting materials are highly desirable. Easy to handle and reusable catalysts based on earth-abundant metals are especially attractive for these syntheses. We report here on the synthesis of 3,4-dihydro-2H-pyrroles via the hydrogenation and cyclization of nitro ketones. The latter are easily accessible from three components: a ketone, an aldehyde and a nitroalkane. Our reaction has a broad scope and 23 of the 33 products synthesized are compounds which have not yet been reported. The key to the general hydrogenation/cyclization reaction is a highly active, selective and reusable nickel catalyst, which was identified from a library of 24 earth-abundant metal catalysts. |
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Keywords: | catalysis hydrogenation multicomponent reaction N-heterocycles nickel |
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