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Research Article

Knoevenagel reaction promoted by functional ionic liquids with primary and tertiary amines

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Article: 2337743 | Received 11 May 2022, Accepted 27 Mar 2024, Published online: 09 Apr 2024
 

ABSTRACT

Functional ionic liquids have been widely used in the fields of synthetic chemistry, analytical chemistry, electrochemistry and material chemistry owing to their excellent properties such as easy structure modification and adjustable properties. In this work, a series of basic functionalized ionic liquids were prepared from 1, 4-diazabicyclo [2.2.2] octane (DABCO) or hexamethylenetetramine (HMTA) with various halogenated hydrocarbons, then these functional ionic liquids and water were used as solvent-catalyst system in the Knoevenagel reaction of various aldehydes with ethyl cyanoacetate or malononitrile, the influence of the structure of the ionic liquid and the content of water was investigated. The results showed that the composite solvent-catalyst system mixed by the functional ionic liquid N-(3-aminopropyl)-1,4-diazabicyclo [2.2.2] octane bromide with water can effectively promote the Knoevenagel reaction and the alkalinity of amine and hydrogen bond play an important role. Aromatic aldehydes with electron-donating or electron-withdrawing groups can obtain the target product at an excellent yield (79-99%). It is worth noting that the polycyclic aromatic aldehydes with high steric hindrance, 86%-95% yields of the object products were also obtained after 15 h-25 h. Furthermore, the catalyst could be reused for 6 times without any loss in its catalytic activity.

The composite solvent-catalyst system mixed by the Functional ionic liquid N-(3-aminopropyl)-1,4-diazabicyclo[2.2.2]octane bromide with water can effectively promote the Knoevenagel reaction, even for the electron-rich aromatic aldehydes with poor reactivity, high yields of the target products and fast reaction rate were also obtained at room temperature.

GRAPHICAL ABSTRACT

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

We are grateful for financial support for this work from the Natural Science Foundation of Shanxi Province [No. 201601D102015] and the Fund for Shanxi ‘1331 Project’ [2021-2023].