In the present work, a mild and highly efficient method for protection of aldehydes with acetic anhydride in the presence of high-valent titanium (IV) salophen trifluoromethanesulfonate, [Ti-IV(salophen)(OTf)(2)], at room temperature is reported. Under these conditions, different aldehydes bearing electron-withdrawing and electron-donating substituents were reacted with acetic anhydride and the corresponding 1,1-diacetates were obtained in good to excellent yields. The results showed that the yields were higher for aldehydes bearing electron-withdrawing substituents such as nitro, chloro, bromo and 3-methoxy, while aldehydes containing electron donating groups such as 4-methoxy and 4-methyl produced the lower yields. The catalyst was reused several times without loss of its catalytic activity. (C) 2012 Elsevier B. V. All rights reserved.