Hi Dawid Janasik, I found a rather simple method in the reference shown below. It states: "Aromatic nitro compounds can be conveniently reduced to the corresponding primary amines in the presence of S 8 under solvent-free conditions in excellent yields. Alumina supported NaOH catalyses this transformation. Chemoselectivity was observed in the reduction of the nitro group in the presence of phenol, carboxylic acid, aldehyde, and benzyl halide groups." Unfortunately I don't have access to the full text.
Article Efficient Reduction of Nitroarenes to the Corresponding Anil...