SELECTIVE SYNTHESIS OF 1,3-DIALKYL-4-NITRO-1,2,3-TRIAZOLIUM SALTS FROM 1-ALKYL-4-NITRO-1,2,3-TRIAZOLES AND DIALKYL SULFATES
DOI:
https://doi.org/10.1007/6561Keywords:
C-nitro-1, 2, 3-triazoles, 3-triazolium salts, quantum-chemical calculations, quaternization, X-ray crystallographyAbstract
The process of alkylation of 1-alkyl-substituted 4-nitro-1,2,3-triazoles with dimethyl and diethyl sulfates has been studied. The structures of the N,N’-dialkyl-C-nitro-1,2,3-triazolium alkylsulfates and perchlorates has been confirmed by IR, 1H and 13C NMR spectroscopy. Alkylation with an excess of dialkyl sulfate occurred regioselectively at N-3 with the formation of 1,3-dialkyl-4-nitro-1,2,3-triazolium salts, which is in agreement quantum-chemical calculations of the relative stability of the corresponding isomeric cations. The molecular and crystal structures of the first example of this type of salt – 1,3-diethyl-4-nitro-1,2,3-triazolium perchlorate – have been determined by X-ray crystallography. Nitrotriazolium salts with mixed alkyl substituents – 3-ethyl-1-methyl- and 1-ethyl-3-methyl-4-nitro-1,2,3-triazolium salts – have been synthesized an studied for the first time.
How to Cite
Ivashkevich, O. A.; Matulis, Vadim E.; Lyakhov, A. S.; Grigorieva, I. N.; Gaponik, P. N.; Sukhanov, G. T.; Filippova, Yu. V.; Sukhanova, A. G. Chem. Heterocycl. Compd. 2009, 45, 1218. [Khim. Geterotsikl. Soedin. 2009, 1519.]