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Catalytic cascade gas-phase heterocyclization of lactic acid and aniline into quinolones over mesoporous Hβ zeolite

Cascade reactions are an important synthetic strategy for efficient and rapid access to molecular complexity in chemical synthesis. In this study, the vapor-phase cascade heterocyclization was further developed, starting with the coupling of biomass-derived lactic acid with aniline to yield high-val...

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Published in:Reaction chemistry & engineering 2024-07, Vol.9 (8), p.2197-227
Main Authors: Liang, Jun-Jie, Wu, Fen, Chen, Zi-Tuo, Xiang, Tao, Wang, Chu-Hui, Li, Li-Jun, Zhou, Cong-Shan, Li, An
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container_end_page 227
container_issue 8
container_start_page 2197
container_title Reaction chemistry & engineering
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creator Liang, Jun-Jie
Wu, Fen
Chen, Zi-Tuo
Xiang, Tao
Wang, Chu-Hui
Li, Li-Jun
Zhou, Cong-Shan
Li, An
description Cascade reactions are an important synthetic strategy for efficient and rapid access to molecular complexity in chemical synthesis. In this study, the vapor-phase cascade heterocyclization was further developed, starting with the coupling of biomass-derived lactic acid with aniline to yield high-value quinoline derivatives. Mesoporous Hβ zeolite was employed as an eco-friendly heterogeneous catalyst, which was prepared via zeolitic dissolution-recrystallization treatment to generate abundant mesopore volume. The assessment of the catalyst activity and stability confirmed that the presence of mesopores within the zeolite significantly improved the life of the catalyst. This enhancement was primarily attributed to the facilitated diffusion of the bulky quinoline products through the pore channels of the mesoporous Hβ zeolite, which mitigates the formation of the coke deposits. Notably, the deactivation of the catalyst was reversible, and its catalytic activity could be almost entirely restored through simple calcination in air to eliminate the coking. Furthermore, this work elucidated the plausible mechanisms relating to the generation of diverse quinoline derivatives and byproducts from the reaction between lactic acid and aniline, which contribute to a better understanding of the complex reaction pathways involved in this cascade synthetic approach. High-value quinoline derivatives were synthesized by vapor-phase cascade heterocyclization via the coupling of biomass-derived lactic acid with aniline, using mesoporous HBeta zeolites as a green and efficient heterogeneous catalyst.
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source Royal Society of Chemistry Journals
subjects Aniline
Cascade chemical reactions
Catalysts
Catalytic activity
Chemical reactions
Chemical synthesis
Coking
Complexity
Coupling (molecular)
Lactic acid
Quinoline
Recrystallization
Zeolites
title Catalytic cascade gas-phase heterocyclization of lactic acid and aniline into quinolones over mesoporous Hβ zeolite
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