New room temperature ionic liquids - choline derivatives were prepared by Menschutkin reaction with alkyl chloromethyl ethers and anion changed to bis(trifluoromethylsulfonyl) amide ion. The newly obtained butoxymethyl(2-hydroxyethyl)dimethylammonium bis(trifluoromethanesulfonyl)amide was successfully tested as a solvent for O-acylation in two-phase reaction system. The ionic liquid-catalyst system was recycled and reused.
Several new quaternary ammonium chlorides, analogues of choline, were prepared by reaction of 2-(dimethylamino)ethanol and its derivatives with chloromethyl alkyl ethers. The obtained chlorides were examined in respect to their antielectrostatic effects: the surface resistance and half decay time on polyethylene film were measured. Application of rough set theory permitted to perform a comprehensive analysis of data and detection of structural-activity relationships. The obtained chlorides showed high antielectrostatic properties. The most active were quaternary ammonium chlorides with 11 and 12 carbon atoms in alkyl chain.
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