Synthesis of 5-Nitro-1,2,4-Triazol-3-One Via: Conventional Heating, Microwave and Ultrasonication

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引用次数: 1

Abstract

In this laboratory experiment 2,4-dihydro-3H-1,2,5-Triazol-3-one(TO) was synthesized using mixture of semicarbazide hydrochloride(SC.HCl) and formic acid in 1:3 mole ratio. TO was further nitrated using 70% nitric acid (HNO3) to produce2,4-dihydro-3H-5-nitro-1,2,5-triazol-3-one(NTO). For the nitration reaction three techniques were employed: conventional heating, microwave assisted and ultrasound assisted reaction. It was found that the extent of gases generation during the reaction was reduced when microwave and ultrasound was employed as compared to the conventional heating method. The time taken for the completion of the reaction was only 15 min when microwave was used.
5-硝基-1,2,4-三唑-3-酮的常规加热、微波和超声合成
本实验以盐酸氨基脲(SC.HCl)与甲酸的混合物为原料,以1:3摩尔比合成2,4-二氢- 3h -1,2,5-三唑-3-酮(TO)。用70%硝酸(HNO3)进一步硝化生成2,4-二氢- 3h -5-硝基-1,2,5-三唑-3-酮(NTO)。对硝化反应采用了常规加热、微波辅助和超声辅助三种技术。结果表明,与传统的加热方法相比,采用微波和超声波加热可以减少反应过程中产生气体的程度。使用微波时,反应完成时间仅为15分钟。
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