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Potassium iodide–polyethylene glycol catalyzed cycloaddition reaction of epoxidized soybean oil fatty acid methyl esters with CO(2)

Nowadays, the clean production of bio-based products and fixation of carbon dioxide (CO(2)) are highly desirable. In this work, carbonated fatty acid methyl esters have been successfully prepared in 99% yield by cycloaddition of CO(2) with bio-based epoxidized methyl soyates. This was accomplished w...

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Detalles Bibliográficos
Autores principales: Liu, Wei, Lu, Guanghui, Xiao, Bing, Xie, Chenfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085569/
https://www.ncbi.nlm.nih.gov/pubmed/35548747
http://dx.doi.org/10.1039/c8ra05947k
Descripción
Sumario:Nowadays, the clean production of bio-based products and fixation of carbon dioxide (CO(2)) are highly desirable. In this work, carbonated fatty acid methyl esters have been successfully prepared in 99% yield by cycloaddition of CO(2) with bio-based epoxidized methyl soyates. This was accomplished with a simple and cheap catalyst system of polyethylene glycol 400 (PEG-400) and potassium iodide (KI) under solvent-free conditions. Experimental parameters such as the molar ratio of polyethylene glycol to metal halide, catalyst loading, reaction temperature, reaction time and CO(2) pressure were systematically evaluated. The PEG-400 and KI co-catalysts (4 mol%) could significantly promote the cycloaddition of CO(2) with internal epoxides (epoxidized methyl soyates) to produce carbonated fatty acid methyl esters. FT-IR and NMR analyses were used to confirm the product, and 99% yield of the five-membered cyclic carbonated methyl soyates was obtained at 120 °C with 3.0 MPa pressure of CO(2) for 20 h. This method provides a cleaner approach for the production of bio-based products.