Electroreduction of N-methylphthalimide in room temperature ionic liquids under insonated and silent conditions

Constanza Villagrán, Craig E. Banks, William R. Pitner, Christopher Hardacre*, Richard G. Compton

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The selective electroreduction N-methylphthalimide to 3-hydroxy-2-methyl- isoindolin-1-one has been performed in ionic liquids using phenol as a proton donor under silent and ultrasonic conditions. A significant increase in the rate of electroreduction is shown using ultrasonic activation and in addition high current efficiencies were observed. Some decomposition of the ionic liquid was found to have occurred under exposure to ultrasound.

    Original languageEnglish
    Pages (from-to)423-428
    Number of pages6
    JournalUltrasonics Sonochemistry
    Volume12
    Issue number6
    DOIs
    Publication statusPublished - Aug 2005

    Keywords

    • Electroreduction
    • Electrosynthesis
    • Ionic liquid
    • N-Methylphthalimide
    • Sonoelectrochemistry

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