Acid clay minerals as eco-friendly and cheap catalysts for the synthesis of β-amino ketones by Mannich reaction
Autor: | Elena Pérez-Mayoral, Beatriz González-Rodríguez, María Virtudes Morales-Vargas, Fernando Gómez-Sanz, M.L. Rojas-Cervantes |
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Rok vydání: | 2017 |
Předmět: |
010405 organic chemistry
Imine Cyclohexanone Geology 010402 general chemistry 01 natural sciences 0104 chemical sciences Catalysis chemistry.chemical_compound Aniline chemistry Geochemistry and Petrology Michael reaction Organic chemistry Lewis acids and bases Brønsted–Lowry acid–base theory Mannich reaction |
Zdroj: | Applied Clay Science. 143:250-257 |
ISSN: | 0169-1317 |
DOI: | 10.1016/j.clay.2017.03.033 |
Popis: | The characterization and catalytic performance of different smectites, one raw saponite and some commercial montmorillonites, exhibiting mesoporous and acid character are herein reported. The catalysts under study are able to catalyze efficiently via Mannich-type reactions the synthesis of β-amino ketones, which are important building blocks for the drugs synthesis and biologically active natural products. Montmorillonite K10 (Mt-K10) was the most efficient catalyst for the Mannich reaction between the pre-formed imine, N-benzylideneaniline, and cyclohexanone resulting in a recyclable catalyst for at least three catalytic cycles without activity loss. Almost quantitative yield to the β-amino carbonyl compound was obtained after 240 min when operating under the most favorable conditions. The catalytic performance of the smectites seemed to be influenced by their porosity, but also by both Bronsted and Lewis acid site concentrations. In fact, the concentration of the Lewis acid catalytic sites would be the key in the Michael addition of cyclohexanone to the imine, although the Bronsted acid sites contribution cannot be neglected. The β-amino carbonyl compound was also synthesized in an excellent yield (86%) in only 15 min of reaction time through the one-pot three component reaction, by reaction between benzaldehyde, aniline and cyclohexanone. |
Databáze: | OpenAIRE |
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