Sodium hydride promoted O-alkylation of 2-[(4-t-butyldimethylsilyloxy)phenyl]ethan-1-ol with 1-bromo-2-(bromomethyl)-4,5-dimethoxybenzene depend on the solvent used in the coupling reaction. Mixtures of 2-[4-(2-bromo-4,5-dimethoxybenzyloxy)phenyl]-1-t-butyldimethylsilyloxyethane and 2-[4-(2-bromo-4,5-dimethoxybenzyloxy)phenyl] ethan-1-ol (in DMF), or 2-[4-(2-bromo-4,5-dimethoxybenzyloxy)phenyl]-1-t-butyldimethylsilyloxyethane and 4-[2-(2-bromo-4,5-dimethoxybenzyloxy)ethyl]phenol (in THF), were detected. These results can be explained by an unusual intermolecular silyl migration reaction.
(a) árias-PérezM.S., LópezM.S., and SantosM.J., J. Chem. Soc., Perkin Trans 2, 2002, 1549; (b) T. Yamazaki, T. Oniki and T. Kitazume, Tetrahedron, 1996, 52, 11753; (c) Z.Q. Zhao, L.Z. Peng and Y.L. Li, Chin. Chem. Lett., 2005, 16, 290.
11.
(a) EvansD.A., IlligC.R., and SaddlerJ.C., J. Am. Chem. Soc., 1986, 108, 2478; (b) Y.-Y. Ku, T. Grieme, P. Raje, P. Sharma, S.A. King and H.E. Morton, J. Am. Chem. Soc., 2002, 124, 4282.