Related Experiment Video
Updated: Jan 12, 2026

Preparation of Binary and Ternary Deep Eutectic Systems
Published on: October 31, 2019
Microwave-Assisted Organic Syntheses in Deep Eutectic Solvents: A Win-Win Association for Sustainable Chemistry
Pierre-Olivier Delaye1, Chefikou Salami1, Emilie Thiery1
1Laboratoire Synthèse et Isolement de Molécules Bioactives (SIMBA, UR 7502), Université de Tours, Faculté de Pharmacie, Tours, France.
None:
The 12 principles of green chemistry guide the scientific community toward the development of chemical processes that are more respectful of the environment and safer for human health. In organic synthesis, this mainly involves the use of sustainable alternatives to conventional organic solvents, energy-efficient processes, and waste minimization. In this context, this review focuses on the use of deep eutectic solvents (DES) in microwave-assisted organic synthesis. Indeed, DES, due to their nonvolatility, nonflammability, and low toxicity compared to conventional organic solvents, are considered desirable "green solvents" for the development of environmentally friendly processes. Moreover, their physicochemical properties make them ideal media for microwave heating. Thus, all organic syntheses using DES as solvent and microwave heating documented in the literature are reported, including heterocycle synthesis, nitrogen quaternization reactions, 5-hydroxymethylfurfural production, Knoevenagel reactions, and miscellaneous transformations. The recyclability of DES-based systems and their scalability, where applicable, are reported. Mechanistical considerations when DES are involved are also described. Compared with conventional heating methods, microwave heating of DES media generally results in good yields and a significant reduction in reaction times. This DES-MW combination appears promising for more sustainable organic syntheses.
Related Concept Videos
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Solvents
A...
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
E2 Reaction: Kinetics and Mechanism

