Heterogeneous Beckmann rearrangements catalyzed by a sulfonated imidazolium salt of phosphotungstate

Xuan Zhang, Dan Mao, Yan Leng, Yu Zhou, Jun Wang

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

Abstract

The heteropolyanion-based ionic liquid (IL) material [MIMPS] 3PW12O40, propane sulfoacid-functionalized imidazolium salt of phosphotungstate, was used as a solid catalyst for liquid-phase Beckmann rearrangements of ketoximes in the presence of zinc chloride. The resultant liquid-solid biphasic rearrangement reaction of cyclohexanone oxime shows a high yield 83 % with good recyclability. The testing of control catalysts, reaction conditions, oxime substrates, and recycling property were carried out and the results are discussed. Graphical Abstract: The heteropolyanion-based ionic liquid (IL) material [MIMPS]3PW 12O40, propane sulfoacid-functionalized imidazolium salt of phosphotungstate, was used as a solid catalyst for liquid-phase Beckmann rearrangements of ketoximes in the presence of zinc chloride. The resultant liquid-solid biphasic rearrangement reaction of cyclohexanone oxime shows a high yield 83% with good recyclability. The testing of control catalysts, reaction conditions, oxime substrates, and recycling property were carried out, and the results are discussed.[Figure not available: see fulltext.]

Original languageEnglish
Pages (from-to)193-199
Number of pages7
JournalCatalysis Letters
Volume143
Issue number2
DOIs
StatePublished - Feb 2013

Keywords

  • Beckmann rearrangement
  • Caprolactam
  • Cyclohexanone oxime
  • Ionic liquid
  • Phosphotungstate

Fingerprint

Dive into the research topics of 'Heterogeneous Beckmann rearrangements catalyzed by a sulfonated imidazolium salt of phosphotungstate'. Together they form a unique fingerprint.

Cite this