Direct Catalytic Conversion of Furfural to Furan‐derived Amines in the Presence of Ru‐based Catalyst
The production of amine intermediates from biomass is capturing increasing attention. Herein, a simple and efficient preparation of l furan‐derived amines was developed [e.g., 1‐(furan‐2‐yl)‐4‐methylpentan‐2‐amine] with high yield (up to 95 %) from (E)‐1‐(furan‐2‐yl)‐5‐methylhex‐1‐en‐3‐one. The cata...
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Veröffentlicht in: | ChemSusChem 2020-04, Vol.13 (7), p.1699-1704 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The production of amine intermediates from biomass is capturing increasing attention. Herein, a simple and efficient preparation of l furan‐derived amines was developed [e.g., 1‐(furan‐2‐yl)‐4‐methylpentan‐2‐amine] with high yield (up to 95 %) from (E)‐1‐(furan‐2‐yl)‐5‐methylhex‐1‐en‐3‐one. The catalyst used was Ru/C, and it was recyclable up to the fourth cycle. To further realize cost‐efficiency, a one‐reactor tandem concept was attempted. To this aim direct reaction from furfural was investigated. A high yield (74 %) towards 1‐(furan‐2‐yl)‐4‐methylpentan‐2‐amine could be achieved starting directly from furfural in the presence of methyl isobutyl ketone, NH3, H2, and Ru/C catalyst.
Green amines: Catalytic conversion of furfural to primary amines is achieved with high yield (74 %) by a one‐reactor two‐step process in the presence of Amberlyst 16 and Ru/C based catalysts. The hydrogenation of C=C bonds together with the reductive amination of carbonyl groups at mild reaction conditions is performed using ammonia and hydrogen. |
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ISSN: | 1864-5631 1864-564X |
DOI: | 10.1002/cssc.202000003 |