Search

The synthesis of a new alkylmethylimidazolium ionic liquid wherein the alkyl group is functionalized with dihexylphosphine oxide moiety at the terminal position has been achieved in four steps from 1-methylimidazole. This hybrid ionic liquid effectively catalyzed the nucleophilic fluorination of primary alkyl mesylates under mild conditions using CsF as the fluoride source with a faster rate compared to butylmethylimidazolium mesylate. The hybrid catalyst was recycled 5 times without compromising the yield and purity of the product. The nucleophilic fluorination has been used for the synthesis of diethyl 2-(5-fluoropentyl)-2-methyl malonate, a precursor of 18 F isotopomer of an apoptosis imaging agent and the protected form of O -(2′-fluoroethyl)- l -tyrosine, a 18 F isotopomer of a tumor imaging agent. [ABSTRACT FROM AUTHOR]

A series of different fluorine-substituted compounds is synthesized by fluorination of primary alkyl mesylates using a new alkylmethylimidazolium ionic liquid as effective catalyst. [ABSTRACT FROM AUTHOR]