4.7 Article

An eco-friendly innovative halide and metal-free basic ionic liquid catalyzed synthesis of tetrahydrobenzo [b] pyran derivatives in aqueous media: A sustainable protocol

Journal

JOURNAL OF MOLECULAR LIQUIDS
Volume 345, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.molliq.2021.117867

Keywords

Pyran; Ionic liquid; Aq. media; Metal-free catalyst

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A novel imidazolium-based basic ionic liquid [PEMIM][OH] was synthesized for the efficient and recyclable multicomponent synthesis of tetrahydrobenzo[b]pyran derivatives, showing high yields in aqueous media. The use of halide and metal-free catalyst establishes a sustainable process, while cost-effective isolation of pure products was achieved by avoiding column chromatography and recrystallization.
A novel imidazolium-based highly efficient, recoverable, and reusable basic ionic liquid [PEMIM][OH] was synthesized using a very simple approach. This ionic liquid was employed as a catalyst for the multicomponent synthesis of tetrahydrobenzo[b]pyran derivatives by the condensation of dimedone, malononitrile and various substituted aldehydes as key starting materials in aqueous media. Novelty, the efficacy of the catalyst, high yields of desired products, greener approach, high atom economy and use of aqueous media make this protocol worthwhile. The inventive idea of employing halide and a metal-free ionic liquid catalyst establishes this as a sustainable process. The cost-effective isolation of pure, high yielded desired product by sidestepping the column and recrystallization technique was also demonstrated in this protocol. A plausible mechanism for the formation of tetrahydrobenzo [b] pyran is proposed. The novel catalyst and synthesized compounds were characterized by using various analytical techniques such as FTIR, H-1 NMR, C-13 NMR, DEPT-135, LC-Mass, Elemental, HSQC, HPLC, TG-DSC, TG-DTG and single crystal XRD analysis. (C) 2021 Elsevier B.V. All rights reserved.

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