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Abstract
The synthesis of isothiocyanato esters appended to (polyethylene glycol)-ionic liquid phases is reported. The starting task-specific ionic liquids (TSILs) were functionalized in good yields with bromoacetic acid or 4-chlorobutyroyl chloride by usual esterification reaction conditions. In the second step, the isocyanato esters appended to TSILs were obtained by displacement with potassium thiocyanate in refluxing anhydrous MeCN. The isothiocyanato-TSILs were characterized by NMR (1H, 13C), mass spectrometry (MS) and IR spectroscopy.
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