4.6 Article

Studies on mild catalytic synthesis of methyl acrylate via one-step aldol reaction

Journal

AICHE JOURNAL
Volume 64, Issue 4, Pages 1359-1372

Publisher

WILEY
DOI: 10.1002/aic.16022

Keywords

methyl acrylate; aldol reaction; mechanism; kinetic; thermodynamic

Funding

  1. National Natural Science Foundation of China [21676270, 21576261]
  2. National Science Fundation for Excellent Young Scholars [21422607]
  3. National Key Projects for Fundamental Research and Development of China [2016YFB0601303]
  4. NSFC-Key Projects of Shanxi Coal Based Low Carbon Joint Foundation [U1610222]
  5. CAS/SAFEA International Partnership Program for Creative Research Teams

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One-step catalytic synthesis of methyl acrylate from methyl acetate and trioxane, with 90.7% yield and 91.8% selectivity, was realized at 10-25 degrees 5. NMR analysis confirmed the ester enolization with generation of [i-Pr2EtN-H](+)[TfO](-) in the presence of i-Pr2EtN and Bu2BOTf, which was affected by solvent and base. The depolymerization of trioxane into formaldehyde was catalyzed by Bu2BOTf. The in-situ catalytic mechanism and efficiency of [i-Pr2EtN-H](+)[TfO](-) was determined and analyzed. Mechanism-based kinetic and thermodynamic studies were conducted for better understanding of this route. Also the primary process design and product separation simulation were carried out. (c) 2017 American Institute of Chemical Engineers AIChE J, 64: 1359-1372, 2018

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