I have an idea.
Acetone in concentrated sulfuric acid is dehydrated and polymerized into mesitylene (1,3,5-trimethylbenzene). With three activating groups in set
positions, mesitylene would nitrate more easily under less rigorous conditions than toluene, and the resulting trinitromesitylene would have only one
isomer.
On its own, TNM sucks, but the methyl groups could then be oxidized to carboxylic acid groups with dichromate or permanganate in sulfuric acid, then
the product could be decarboxylated via heat to sym-trinitrobenzene, which is superior to sym-TNT in every way, save for TNT's easier synthesis.
Does anyone have any comments on this proposed procedure? |