Herein, we present a novel approach for the halide-free, continuous-flow preparation of hydrophobic ionic liquids (ILs) relying on the bis(trifluoromethanesulfonyl)imide (bistriflimide, NTf2 -) anion. The simple yet fast two-step synthetic route, which involves the formation of different alkyl bistriflimides (R4NTf2), followed by the quaternization with an amine nucleophile, led to the desired ILs in high yields and excellent purities without any byproduct formation. The variable alkyl chain (R4) length and the broad range of the applicable nucleophiles (R1R2R3N) offer considerable flexibility to the synthetic protocol. The quaternization can be performed under solvent-free conditions; moreover, the homogeneous nature of these reactions allows the application of modern continuous-flow technologies. Given these advantages, the methodology can afford not just a fast and efficient alternative for the conventional synthesis of such compounds with reduced waste water production but their negligible halide content might provide a significantly broader application range of the IL products, especially for the field of materials science.
© 2022 The Authors. Published by American Chemical Society.