A green, facile, fast, and high throughput reusable catalytic reduction process was developed for the large-scale reduction of tris(p-nitrophenyl)amine to its corresponding amino-compound, tris(p-aminophenyl) amine (TAPA). The homogenous AgNPs and NaBH₄ were used as the H-transfer catalyst and the H-donor compound, respectively. The successful reduction of TNPA was investigated by FT–IR, EDX, and XRD analysis, and its optical properties were checked by the UV–Visible and FL spectroscopies. Factors affecting the reduction yield including, temperature, reaction time, mmol of NaBH₄, and catalyst volume, were optimized. Although the AgNPs are homogenous, both TNPA and TAPA are insoluble in water (AgNPs), hence the reduction process is heterogeneous. The importance of the heterogeneous reduction of TNPA was investigated, indicated that the reduction yield reached its maximum value when TNPA heterogeneously reduced on the surface of AgNPs. The reduction yield at optimal conditions was calculated at about 98.0% for the first and 72.0% after the 6^6th operational cycle, respectively. The mechanism of thereduction process was also established, indicated that the process works through a possible Langmuir–Hinshelwood mechanism. The easy recovery and excellent reusability of homogenous AgNPs along with high reaction yield reveal the power of the proposed method for the reduction of nitro-compounds.