Sustainable Microwave‐Enhanced Synthesis of 2‐Substituted Benzofurans From o‐Alkynylanisoles in Acidic Deep Eutectic Solvents
Articolo
Data di Pubblicazione:
2026
Citazione:
Sustainable Microwave‐Enhanced Synthesis of 2‐Substituted Benzofurans From o‐Alkynylanisoles in Acidic Deep Eutectic Solvents / A. Gritti, A. Sita, M. Goudarzi, S. Fedeli, E. Lepore, D. Nava, M. Tiecco, A. Caselli, V. Pirovano, G. Abbiati. - In: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. - ISSN 1434-193X. - (2026), pp. e70463.1-e70463.9. [Epub ahead of print] [10.1002/ejoc.70463]
Abstract:
The research on alternative media for organic transformations remains a highly demanding topic. In this paper, we describe a sustainable, microwave-enhanced approach to 2-substitued benzofurans starting from substituted o-alkynylanisoles. The method involves the use of an acidic deep eutectic solvent that acts simultaneously as reaction medium and catalyst. The optimized reaction conditions are quite mild (100°C) and the process is complete within 3 h. The reaction setup is simple and does not require an inert atmosphere. Under these conditions, seventeen benzofurans were synthesized in yields of up to 90%. A plausible reaction mechanism has been proposed and supported by headspace GC analyses. To evaluate the sustainability of the process Sheldon's simple environmental factor was also calculated.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
DES; benzofurans; alkynes; anisoles; heterocycles; sustainability; microwaves;
Elenco autori:
A. Gritti, A. Sita, M. Goudarzi, S. Fedeli, E. Lepore, D. Nava, M. Tiecco, A. Caselli, V. Pirovano, G. Abbiati
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