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Synthesis of Esters Via a Greener Steglich Esterification in Acetonitrile
Published on: October 30, 2018
Deep Eutectic Solvent-Type Mixture as a Green Catalyst in the Solvent-Free Cycloaddition of CO2 and Epoxides
Tatiana Martí1,2, Xavier Marset1, Celia Guillem2
1Departamento de Química Orgánica, Instituto de Síntesis Orgánica (ISO), Facultad de Ciencias, Universidad de Alicante, Alicante, Spain.
None:
A sustainable approach for CO2 valorization through cycloaddition with epoxides is proposed to synthesize cyclic carbonates, recognized as compounds in green chemistry and industrial applications. A novel deep eutectic solvent (DES)-type catalyst, comprising a mixture of tetrabutylammonium iodide and levulinic acid in a 1:1.5 molar ratio, is introduced and thoroughly characterized. This mixture demonstrates efficiency under mild and solvent-free conditions, providing improved selectivity and conversion rates compared to other related catalysts. This catalyst system (1.4 mol%) operates at atmospheric pressure, avoiding the need for high-pressure equipment while enhancing scalability. Furthermore, this procedure is considered an ideal approach from both economic and ecological perspectives, due to its 100% atom economy and reduced environmental impact, offering a promising, metal-free and low-toxicity alternative. Additionally, the DES-type catalytic system can be recycled for at least three consecutive cycles while maintaining significant activity. Quantum chemistry calculations provide mechanistic insights supporting experimental findings. Overall, these findings underscore the potential of DES-based systems to advance CO2 utilization technologies, contributing to circular carbon strategies and sustainable chemical synthesis.
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Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...

