Related Experiment Video
Updated: May 15, 2025

A Microwave-Assisted Direct Heteroarylation of Ketones Using Transition Metal Catalysis
Published on: February 16, 2020
Intensification of Ethylene Carbonate Synthesis via Microwave-Induced Phase-Change Cycles
Ioannis Papaioannou1, Athanasios Arampatzis1, Ioanna Tzortzi1,2
1School of Chemical Engineering, National Technical University of Athens, Iroon Polytecneiou 9, Zografou Campus, 157 80, Athens, Greece.
None:
This study reports for the first time on the application of microwave (MW) heating under ambient pressure reflux conditions to intensify the transesterification reaction of ethylene glycol with dimethyl carbonate (DMC) for the synthesis of ethylene carbonate (EC), a relevant industrial compound for polycarbonate products, lubricants and li-ion batteries. Conventional heating (CH) methods often require high-temperature autoclave systems to achieve elevated temperatures and suppress vaporization of the reactant DMC (bp ≈ 90 °C). However, these systems usually entail extended reaction times and significant process cost. It is demonstrated that application of the MW-assisted reflux technique to the aforementioned transesterification reaction intensifies the energy transfer rate to the reactor by leveraging on the polarity of the reactive mixture and enhances phase transition of the lowest boiling point by-product (MeOH), thereby achieving 81% EC yield in half the time required under CH reflux conditions to reach only 52% EC yield. Further, compared to CH, MW heating enables 20-fold lower catalyst loading for comparable EC yields, 9-fold decrease in energy consumption per mole EC, and 92% reduction in energy consumption during the mixture preheating stage.
More Related Videos
Related Concept Videos
Cycloaddition Reactions: MO Requirements for Photochemical Activation
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.
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Thermal and Photochemical Electrocyclic Reactions: Overview
Cycloaddition Reactions: MO Requirements for Thermal Activation
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...

