Related Experiment Video
Updated: May 14, 2025

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyltroponeiron
Published on: August 12, 2019
Mechanochemical Nitration Studies of Aminotriazole Compounds
Jie Zhou1, Yang Zhao2, Jiaheng Wang1
1School of Materials and Chemistry, Southwest University of Science and Technology, Mianyang 621010, People's Republic of China.
Abstract:
In order to promote the green development of the nitration process of energy-containing materials and to reduce the environmental pollution and resource waste caused by the traditional nitration reaction. We used a solvent-free mechanochemical reaction to nitrify 3-amino-1,2,4-triazole and 3,5-diamino-1,2,4-triazole and successfully obtained 3-nitro-1,2,4-triazole and 3,5-dinitro-1,2,4-triazole by using sodium nitrite and molybdenum trioxide as catalysts. Several parameters affecting the nitration reaction were explored, and the structures of the products were analyzed by combining Gaussian, Multiwfn, and other computational software; also, single crystals of 3,5-dinitro-1,2,4-triazole sodium salt were cultivated and analyzed for their crystal structure and surface properties, and their copper and lead salts were obtained by reacting with metal salts. The present work provides a new idea for the development of green nitration of energy-containing materials.
More Related Videos
07:30A Direct, Regioselective and Atom-Economical Synthesis of 3-Aroyl-N-hydroxy-5-nitroindoles by Cycloaddition of 4-Nitronitrosobenzene with Alkynones
Published on: January 21, 2020
10:42Preparation of N-2-alkoxyvinylsulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines
Published on: January 3, 2018
Related Concept Videos
Electrophilic Aromatic Substitution: Nitration of Benzene
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
Preparation of Amines: Reduction of Oximes and Nitro Compounds
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
2° Amines to N-Nitrosamines: Reaction with NaNO2
Preparation of Amines: Reduction of Amides and Nitriles
Amides can be reduced to primary, secondary, and tertiary amines using catalytic hydrogenation, active metals like Fe,...
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...