Formation of ε-caprolactam via catalytic Beckmann rearrangement using P2O5 in ionic liquids
✍ Scribed by Rex X Ren; Larisa D Zueva; Wei Ou
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 50 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Catalytic Beckmann rearrangement of cyclohexanone oxime in ionic liquids using P 2 O 5 or Eaton's reagent has been investigated. 1-n-Butyl-3-methylimidazolium hexafluorophosphate (bmiPF 6 ) gives superior results to those noted by earlier workers.
📜 SIMILAR VOLUMES
Under mild conditions and without any additional organic solvents, Beckmann rearrangements of several ketoximes were performed in the catalytic media consisting of room temperature ionic liquid based on 1,3-dialkylimidazolium or alkylpyridinium salts and phosphorated compounds. Excellent conversion
## Abstract magnified image A series of novel gemini dicationic acidic ionic liquids (GDAILs), compounds **1**–**3** carrying two SO~3~H groups at the cation moieties and having anions of the type CF~3~SO$\rm{ \_3^ - }$, were synthesized in good yields (__Scheme 1__). Some physicochemical properti