JOURNAL ARTICLE

Reusable Deep Eutectic Solvents for Clean ε-Caprolactam Synthesis under Mild Conditions

Shiqin SunShiwei LiuFengli YuJian ZhangWeiguo XingShitao Yu

Year: 2022 Journal:   ACS Sustainable Chemistry & Engineering Vol: 10 (4)Pages: 1675-1688   Publisher: American Chemical Society

Abstract

A deep eutectic solvent (DES) with adjustable Brønsted acidity was prepared easily by choline chloride (ChCl) and trifluoromethanesulfonic acid (TfOH). The obtained DES [ChCl][TfOH]3 exhibited great stability and excellent catalytic performance in the Beckmann rearrangement reaction as solvent and catalyst. High cyclohexanone oxime (CHO) conversion (100%) and ε-caprolactam selectivity (98.8%) were obtained under mild conditions, such as DESs 0.03 mol, CHO 0.01 mol, 100 °C for 2 h. DES [ChCl][TfOH]3 was easily prepared, recovered, and reused simply for seven runs without noticeable loss of catalytic performance. The free energy (ΔG) and activation energy (Ea) of the reaction were −32.8 and 39.82 kJ mol–1, respectively. And, DFT results showed that the intermolecular hydrogen bond between ChCl and TfOH improved the thermal stability of DES (the six-membered ring structure formed containing Cl and N atoms) and provided a good sponge effect for the active hydrogen catalytic center required for the reaction (the hydrogen bond formed by Cl and hydroxyl). This process offered several advantages including good yields, short reaction times, and easy catalyst recoveries and makes the DES catalytic system a potentially practical procedure for Beckmann rearrangement.

Keywords:
Beckmann rearrangement Catalysis Caprolactam Chemistry Deep eutectic solvent Cyclohexanone oxime Choline chloride Hydrogen bond Selectivity Solvent Hydrogen chloride Organic chemistry Polymer chemistry Eutectic system Molecule

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Topics

Ionic liquids properties and applications
Physical Sciences →  Chemical Engineering →  Catalysis
Chemical Synthesis and Reactions
Physical Sciences →  Chemistry →  Organic Chemistry
Oxidative Organic Chemistry Reactions
Physical Sciences →  Chemistry →  Organic Chemistry

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