Smiglak, Marcin published the artcileAzolium azolates from reactions of neutral azoles with 1,3-dimethyl-imidazolium-2-carboxylate, 1,2,3-trimethyl-imidazolium hydrogen carbonate, and N,N-dimethyl-pyrrolidinium hydrogen carbonate, Synthetic Route of 14544-45-7, the publication is New Journal of Chemistry (2013), 37(5), 1461-1469, database is CAplus.
Utilizing previously reported synthetic protocols for the halide- and metal-free synthesis of organic salts, we have prepared a new group of imidazolium and pyrrolidinium azolate anion-based salts demonstrating the general applicability of the methodol. and expanding our investigation into non ion exchange routes to potentially energetic ionic liquids Eighteen salts, out of which six exhibit m.ps. below 100 °C, were prepared by a simple decarboxylation reaction, which resulted in clean formation of the new compounds without the need for extensive purification The low stability of the H2CO3 byproduct, and its decomposition to CO2 and H2O in aqueous media, allows for purification of the salts by evaporation only.
New Journal of Chemistry published new progress about 14544-45-7. 14544-45-7 belongs to triazoles, auxiliary class Triazoles, name is 5-Nitro-1H-1,2,3-triazole, and the molecular formula is C20H17FO4S, Synthetic Route of 14544-45-7.
Referemce:
https://en.wikipedia.org/wiki/1,2,3-Triazole,
Triazoles – an overview | ScienceDirect Topics