One-step conversion of xylose to furfuryl alcohol was investigated over Pt catalySts supported on ordered mesoporous SBA-15 bearing-SO3H acid groups. Samples were characterized by SAXRD, FTIR, Si-29 CPNMR, XRF, FE-SEM and TG-MS, and they were all tested in aqueous-phase conversion of xylose in a semi-batch reactor. It was found that the presence of acid sites enhances catalytic activity, confirming that they are also playing a role in xylose cOnversion. A coupled activity of both metal and acid surface centres was thus suggested. The distribution of products was also found to be significantly modified by grafting organosulfonic groups on catalyst surface; while xylitol was the main product on unmodified Pt/SBA-15 catalyst (selectivity of 45%), a remarkable selectivity of 83-87% to furfuryl alcohol was accompliShed over the catalysts Supported on organic-inorganic hybrid mesoporous silica. Additionally, no furfural was detected along the aqueous-phase reaction, evidencing that no remote surface acid sites were playing a sole role. It was suggested that direct highly chemoselective conversion of xylose to furfuryl alcohol takes place on vicinal acid-metal surface sites. Finally, the hybrid catalysts were found to be stable regarding their mesostructure framework upon aqueous-phase processing but acid groups resistance to leaching is still the major challenge for one-pot conversion. (C) 2017 Elsevier B.V. All rights reserved.