Removal of vicinal diols by combination of deoxydehydration and hydrogenation (DODH + HG) was carried out over the mixture of ReO x /CeO 2 and CeO 2 -supported base metals with H 2 as the reducing agent, in order to replace expensive Pd in the ReO x −Pd/CeO 2 catalyst used in previous studies for the same reaction. Similar high activity and selectivity of the mixture catalysts of ReO x /CeO 2 and pre-reduced Ni/CeO 2 were observed for DODH + HG as those of Pd-based catalysts (co-loaded ReO x −Pd/CeO 2 or mixture catalysts of ReO x /CeO 2 + Pd/CeO 2 ), while coloaded ReO x −Ni/CeO 2 catalyst showed almost no activity. The ReO x /CeO 2 + Ni/CeO 2 catalyst system gave 99% yield of tetrahydrofuran from 1,4anhydroerythritol and could be applied to DODH + HG of other diols and polyols such as glycerol, erythritol, and xylitol. Unlike ReO x −Pd/CeO 2 , the activity of the ReO x /CeO 2 + Ni/CeO 2 catalyst decreased in the reuse test, especially before second or later reuses, even when the recovered catalyst was calcined as regeneration. The catalysts were characterized by various methods such as thermal gravimetry−differential thermal analysis, temperatureprogrammed reduction with H 2 , and X-ray absorption fine structure spectroscopy. The deactivated ReO x /CeO 2 + Ni/CeO 2 catalyst after use and the inactive ReO x −Ni/CeO 2 catalyst after reduction had Re−Ni direct bonds, suggesting that the strong interaction between Re and Ni species decreased the activity of ReO x /CeO 2 in the DODH reaction.