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Simulated ageing of 2,4-dinitro-1-ethylbenzene (DNEB) in DMSO in the presence of O2 in a closed system at 85–105°C gave benzylic oxidised products 1-(2,4-dinitrophenyl)ethanol (DNPE) and 2,4-dinitroacetophenone (DNAP), with the latter as the major product. Evidence for the formation of 3-methyl-6-nitro-2,1-benzoisoxazole (an ‘anthranil’), suggested in the literature as a likely decomposition product, is scant. A mechanism with initial H-abstraction to yield an electron-rich benzylic radical as the rate-limiting step is suggested, supported by a small kinetic isotope effect kH/kD ~2 and a reactivity in the order 2,4,6-trinitro-1-ethylbenzene TNEB > DNEB > 4-nitro-1-ethylbenzene (NEB). The activation energy for DNEB oxidation is 40 kJ mol−1, a value that translates to 1% oxidative decomposition of DNEB after ~ 14 d under an O2 atmosphere, or 70 d in air at ambient temperature.

This paper describes the deuterium-labelling of alkylnitroaromatics by base-catalysed exchange with deuterium oxide. As the alkyl protons alpha to the aromatic ring are the most acidic sites in the molecule, regioselective hydrogen isotope exchange at this benzylic location leads to a regiospecifically deuterated product. The exchange labelling takes place in good yields and with high atom% abundance in the presence of an appropriate nitrogen base. Alkylated 2,4-dinitrobenzenes deuterate at room temperature under catalysis by triethylamine, whilst alkylated 2-nitro- or 4-nitrobenzenes and related mono-nitroaromatics require higher temperatures and catalysis by 1,5-diazobicyclo[4.3.0]non-5-ene (DBN). The labelling reactions require an inert gas atmosphere, but otherwise are simple and high yielding with no obvious byproducts. Those compounds in which the benzylic protons are in an ortho-orientation with respect to the nitro group label somewhat more slowly than the analogues where there is a para relationship. In addition, higher alkyl homologues undergo benzylic deuteration at slower rates than methyl.