Cobalt Ion‐Containing DABCO‐Based Ionic Liquid: A Novel and Efficient Catalyst for the Synthesis of 2,3‐Dihydroquinazolin‐4(1 <i>H</i> )‐ones

Abstract [(DABCO) 2 C 3 H 5 OH].CoCl 4 , a novel Lewis acidic ionic liquid, was prepared and properly characterized by a variety of techniques, including Fourier transform infrared (FT‐IR) spectroscopy, thermogravimetric analysis (TGA), X‐ray diffraction (XRD) pattern, energy dispersive X‐ray(EDX) analysis, and field emission scanning electron microscopy (FESEM). Subsequently, the promoting ability of this reagent was investigated in the one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1 H )‐ones through a green and sustainable procedure. Ease of the preparation and reusability of [(DABCO) 2 C 3 H 5 OH].CoCl 4 , short reaction times, excellent yields of the obtained compounds, and solvent‐free nature of the reaction conditions are among the prominent features of the presented protocol.

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Publication Details

Journal
ChemistrySelect
Published
2025-05-01
DOI
https://doi.org/10.1002/slct.202500073
Citations
1
Primary Topic
Quinazolinone synthesis and applications
Type
article
Field-Weighted Citation Impact
0.94
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article

Cobalt Ion‐Containing DABCO‐Based Ionic Liquid: A Novel and Efficient Catalyst for the Synthesis of 2,3‐Dihydroquinazolin‐4(1 H )‐ones

Narges Seyedi, Farhad Shirini, Mohammad Ali Frutan
1 citations
ChemistrySelect
Quinazolinone synthesis and applications
0.94
article

Cobalt Ion‐Containing DABCO‐Based Ionic Liquid: A Novel and Efficient Catalyst for the Synthesis of 2,3‐Dihydroquinazolin‐4(1 H )‐ones

Narges Seyedi, Farhad Shirini, Mohammad Ali Frutan
article en
1 citations

Abstract

Abstract [(DABCO) 2 C 3 H 5 OH].CoCl 4 , a novel Lewis acidic ionic liquid, was prepared and properly characterized by a variety of techniques, including Fourier transform infrared (FT‐IR) spectroscopy, thermogravimetric analysis (TGA), X‐ray diffraction (XRD) pattern, energy dispersive X‐ray(EDX) analysis, and field emission scanning electron microscopy (FESEM). Subsequently, the promoting ability of this reagent was investigated in the one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1 H )‐ones through a green and sustainable procedure. Ease of the preparation and reusability of [(DABCO) 2 C 3 H 5 OH].CoCl 4 , short reaction times, excellent yields of the obtained compounds, and solvent‐free nature of the reaction conditions are among the prominent features of the presented protocol.

ChemistrySelectVol. 10(20)
University of Guilan (IR)
Openalex Percentile: Top 26%
Quinazolinone synthesis and applications
0.94
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