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Polyethylene glycol (PEG) is found to be an inexpensive and non-toxic reaction medium for the microwave-assisted Suzuki cross-coupling of arylboronic acids with aryl halides. This environmentally friendly microwave protocol offers ease of operation and enables recyclability of catalyst and synthesis of a variety of substituted biaryls employing palladium chloride as catalyst and potassium fluoride as the base.

[reaction: see text] An ultrasound-assisted preparation of a series of ambient-temperature ionic liquids, 1-alkyl-3-methylimidazolium (AMIM) halides, which proceeds via efficient reaction of 1-methyl imidazole with alkyl halides/terminal dihalides under solvent-free conditions, is described.

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An efficient solventless protocol for the preparation of a wide variety of ionic liquids is described, which requires a simple exposure of admixed 1-methylimidazole and alkyl halides to microwave irradiation in open glass containers. The details of this clean process using a common household microwave oven, which exploits the newer inverter technology system for better power attenuation, are described. The characterization and thermal stability data on selected ionic liquids and their potential applications are summarized.