The oxidation of cyclohexanol to cyclohexanone with 30% aqueous hydrogen peroxide by using peroxotung-state complexes formed in situ from sodium tungstate di-hydrate and various bidentate organic ligands as the catalysts, without organic solvents, halide and phase transfer catalyst has been carried out. The influence of 13 ligands on the oxidation is investigated. The maximum yield of cyclohexanone is obtained when using 1,10-phenanthroline (96%) and oxalic acid (95%) as the ligand. Very high yields (around 90%) have also been obtained for the instances of using salicylic acid, 3,5-dibromosalicylic acid, and 8-hydro- xylquino-line as ligands. A research to improve the reaction condition using cheap oxalic acid as the ligand indicates that the optimum condition is that the reaction mixture with a molar ratio of cycohexanol:tungstate dihydrate:oxalic acid: 30% H2O2=100:2:2:120 was stirred at 85-90℃ for 12 h. The oxidation of cyclohexanol to cyclohexanone with 30% aqueous hydrogen peroxide by using peroxotung-state complexes formed in situ from sodium tungstate di-hydrate and various bidentate organic ligands as the catalysts, without organic solvents, halide and phase transfer catalyst has been carried out. The influence of 13 ligands on the oxidation is investigated. The maximum yield of cyclohexanone is obtained when using 1,10-phenanthroline (96%) and oxalic acid (95%) as the ligand. Very high yields (around 90%) have also has been obtained for the instances of using salicylic acid, 3,5-dibromosalicylic acid, and 8-hydro-xylquino-line as ligands. A research to improve the reaction condition using cheap oxalic acid as the ligand said that the optimum condition is that the reaction mixture with a molar ratio of cycohexanol: tungstate dihydrate: oxalic acid: 30% H2O2 = 100: 2: 2: 120 was stirred at 85-90 ° C for 12 h.