The
commercially practiced conversion of trimethoxymethylsilane (MTM)
to [OSi(OMe)Me)]<sub><i>n</i></sub> polymers and resins
is assumed to proceed via the silanol (MeO)<sub>2</sub>MeSiOH. Access
to this crucial silanol is gained via the synthesis of (MeO)<sub>2</sub>MeSiONa, the first methoxysilanoate to be crystallographically characterized.
Mild protonation of this silanoate gives (MeO)<sub>2</sub>MeSiOH,
which is shown to condense with (MeO)<sub>2</sub>MeSiOH but not with
MTM. Condensation generates reactive disiloxanols but does not produce
symmetric disiloxanes. Parallel results were obtained with (MeO)<sub>2</sub>PhSiOH