Issue 6, 2002

Ultrasound promoted Suzuki cross-coupling reactions in ionic liquid at ambient conditions

Abstract

Palladium catalyzed Suzuki cross-coupling reactions of halobenzenes including chlorobenzenes with phenylboronic acid have been achieved at ambient temperature (30 °C) in the absence of a phosphine ligand using the ionic liquid 1,3-di-n-butylimidazolium tetrafluoroborate [bbim][BF4] with methanol as co-solvent under ultrasonic irradiation.

Graphical abstract: Ultrasound promoted Suzuki cross-coupling reactions in ionic liquid at ambient conditions

Article information

Article type
Communication
Submitted
11 Dez 2001
Accepted
12 Feb 2002
First published
22 Feb 2002

Chem. Commun., 2002, 616-617

Ultrasound promoted Suzuki cross-coupling reactions in ionic liquid at ambient conditions

R. Rajagopal, D. V. Jarikote and K. V. Srinivasan, Chem. Commun., 2002, 616 DOI: 10.1039/B111271F

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