a study on the condensation reaction of 4-amino-3,5-dimethyl-1,2,4-triazole with benzaldehydes: structure and spectroscopic properties of some new stable hemiaminals
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ID: 254095
2015
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Abstract
Studies on the stable hemiaminals and Schiff bases formation in the reaction of substituted benzaldehydes with primary 3,5-dimethyl-1,2,4-triazole 4-amine were carried out under neutral conditions. These products were investigated by IR, Raman, MS, 1H- and 13C-NMR spectra as well as by X-ray crystallography. The effect of reaction conditions: temperature, polarity of the solvents utilized, substrate concentration and the ortho and para benzaldehyde substituents on the yield of products was also examined.
| Reference Key |
wajda-hermanowicz2015moleculesa
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|---|---|
| Authors | ;Katarzyna Wajda-Hermanowicz;Damian Pieniążczak;Aleksandra Zatajska;Robert Wróbel;Krzysztof Drabent;Zbigniew Ciunik |
| Journal | Journal of ethnopharmacology |
| Year | 2015 |
| DOI |
10.3390/molecules200917109
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| URL | |
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