Chemoselective Cleavage of Si–C(sp<sup>3</sup>) Bonds in Unactivated Tetraalkylsilanes Using Iodine Tris(trifluoroacetate)
Keitaro Matsuoka, Narumi Komami, M. Kojima, Tsuyoshi Mita, Kimichi Suzuki, Satoshi Maeda, Tatsuhiko Yoshino, Shigeki Matsunaga
Abstract
Organosilanes are synthetically useful reagents and precursors in organic chemistry. However, the typical inertness of unactivated Si–C(sp3) bonds under conventional reaction conditions has hampered the application of simple tetraalkylsilanes in organic synthesis. Herein we report the chemoselective cleavage of Si–C(sp3) bonds of unactivated tetraalkylsilanes using iodine tris(trifluoroacetate). The reaction proceeds smoothly under mild conditions (−50 °C to room temperature) and tolerates various polar functional groups, thus enabling subsequent Tamao–Fleming oxidation to provide the corresponding alcohols. NMR experiments and density functional theory calculations on the reaction indicate that the transfer of alkyl groups from Si to the I(III) center and the formation of the Si–O bond proceed concertedly to afford an alkyl-λ3-iodane and silyl trifluoroacetate. The developed method enables the use of unactivated tetraalkylsilanes as highly stable synthetic precursors.