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Mechanism of Friedel–Crafts Acylation Using Metal Triflate in Deep Eutectic Solvents: An Experimental and Computational Study

[Image: see text] In this paper, we develop a method for Friedel–Crafts acylation using metal triflate in deep eutectic solvents. Various metal triflates were tested and provided good to excellent yields of corresponding ketone products. The density functional theory calculation revealed the metal e...

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Detalles Bibliográficos
Autores principales: Nguyen, Minh-Tam Thi, Le, Nghia, Nguyen, Hai Truong, Luong, Tram Diem Vu, Nguyen, Van Kieu Thuy, Kawazoe, Yoshiyuki, Tran, Phuong Hoang, Pham-Tran, Nguyen-Nguyen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835085/
https://www.ncbi.nlm.nih.gov/pubmed/36643563
http://dx.doi.org/10.1021/acsomega.2c03944
Descripción
Sumario:[Image: see text] In this paper, we develop a method for Friedel–Crafts acylation using metal triflate in deep eutectic solvents. Various metal triflates were tested and provided good to excellent yields of corresponding ketone products. The density functional theory calculation revealed the metal effects on the formation of active intermediate acylium triflate as well as the acidic condition. The metal triflate in the deep eutectic solvent can be recovered and reused with a little loss in the catalytic activity.