University of Arizona researchers have developed a novel, one-step, catalyst-free, and solvent-free synthetic process for the nitration of aromatic compounds. This method has been used to prepare 2,4-dinitroanisole, an alternative to trinitrotoluene (TNT), as an ingredient in melt-cast explosive formulations; and dinitrophenyl ethers. This synthetic process can be utilized to produce a variety of nitroaromatic compounds in a fast, straightforward, and more economical fashion than traditional chemical methods.
Background: Traditional synthetic nitration methods often employ catalysts, solvents, or other additives that are harmful to the environment and/or expensive. This synthetic process overcomes these issues by allowing the nitration of various aromatic compounds in a catalyst-free and solvent-free fashion.
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