Selective reduction of nitroaromatic compounds
Abstract
The use of sodium hydrosulphide as a selective reducing agent for aromatic nitro-groups has been investigated with respect to experimental details (including solvent) and yield and ease of purification of product, via studies on the x,y′-dinitrobiphenyls (x= 2–4, y= 2–4). The hydrosulphide-induced reduction is superior to previously reported methods. Its advantages and possible applications are discussed.