Ascribing to the superiority of possessing noteworthy physicochemical
properties, ionic liquids engirdle a scientific interest in research area of chemistry as
green solvent over past few decades. Being constituted entirely of ionic species, these
solvents remain often as fluid at room temperature. The strength of the cation, anion or
the combination of both governs the acidity or basicity of reactive ionic liquids. Due to
some special properties like flexibility, non-volatility, non-corrosive, tunable property,
high thermal stability and recyclability; ionic liquids offer a great potential to replace
conventional solvents in chemical synthesis. Further, the use of acidic or basic ionic
liquids reduces the necessity of using external acid or base along with the solvents.
Therefore, implementation of these ionic liquids in chemical laboratory is widely
accepted as one of the green techniques as it lessens the adverse environmental
impacts.
1,2,3-triazoles are highly desired synthetic molecules in the field of chemical and
pharmaceutical industries as triazole containing moieties possess potent biological
activities such as anti-viral, anti-epileptic, anti-allergic, anti-microbial, anti-cancer,
antituberculosis and anti-HIV properties. Its application is also extended to other areas
such as organic synthesis, polymer science, material science and chemical biology. As
the incorporation of basic condition favors the synthesis of these privileged classes of
compounds from their starting reagents, use of basic ionic liquids as reaction media
provides an alternative and greener approach for their facile construction. This chapter
will discuss triazole synthesis under green conditions by following three different
routes in basic ionic liquid:
• Direct azide-alkyne cycloaddition reactions affording 1,2,3-triazoles.
• Cascade synthesis of triazoles from azides and carbonyl compounds.
• One pot three component reactions leading to 1,2,3-triazoles.
Keywords: 1, 2, 3-triazoles, Anti-microbial, Atom economy, Basic ionic liquid,
Click-chemistry, CuAAC, Cascade synthesis, Green Chemistry, One pot reaction,
Sustainable Solvents.
