Proposed in this paper is an improved Tietze's method to synthesize phenolic O-glycoside. In this method, anhydrousSnCl4instead of trimethylsilyl trifluromethanesulfonate was used as the reaction accelerator, and peracetyl glycoside instead of 1-O-trimethylsilyl acetyl glycoside was used as the starting material to react with three phenolic trimethylsilyl ethers ( Ⅰ a- Ⅰ c). Thus, three kinds of products, namely 1-O-(4-nitrophenyl)-2,3,5-tri- O-acetyl-β-D-ribofuranoside, 1-O-( 4-acetylphenyl ) -2,3,5-tri-O-acetyl-β-D-ribofuranoside, and 1-O-( 4-benzoyloxyphenyl)-2,3,5-tri-O-acetyl-β-D-ribofuranoside, were synthesized, with a shortened synthesis route and at low cost. Moreover, the effects of different Lewis acids, the proportion of the starting materials, the anhydrous SnCl4dosage, and the solvents on the reaction were investigated. The results show that anhydrous SnCl4proves to be an optimal reaction accelerator to the synthesis when the dosage is more than the stoichiometric amount; the suitable molar ratios of the starting materials are respectively nⅠa:nⅡ:nSnCl4=1.0:1.4:1.5,nⅠb:nⅡ:nSnCl4=1.0:1.1:1.4,nIc:nⅡ:nSnCl4=1.0:1.0:1.5; and dried diehloromethane is a suitable solvent for the reaction, while aeeto- nitrile or un-dried diehlorolnethane as solvent may produce the by-product 4-nitrophenyl acetate.