1-(Heteryloxy)silatranes was written by Iovel, I.;Golomba, L.;Popelis, J.;Grinberga, S.;Lukevics, E.. And the article was included in Chemistry of Heterocyclic Compounds (New York)(Translation of Khimiya Geterotsiklicheskikh Soedinenii) in 2000.Safety of 6-Methyl-2-pyridinemethanol This article mentions the following:
Novel heterocyclic 1-derivatives I of silatranes were obtained [R = Et, PhCH2, 2-tetrahydrofurfuryl, 3-pyridinyl, and (6-methyl-2-pyridyl)methyl -]. The optimal synthetic method for these compounds is transesterification of tetraethoxysilane by an equimolar mixture of triethanolamine and a heterocyclic (or aromatic) hydroxyl-containing compound E.g., heating 0.01 mol each PhCH2OH, N(CH2CH2OH)3 and Si(OEt)4 in 14 mL xylene containing 0.2 g KOH at (120-130°) gave 1-benzyloxysilatrane I (R = PhCH2) in 75% yield. In the experiment, the researchers used many compounds, for example, 6-Methyl-2-pyridinemethanol (cas: 1122-71-0Safety of 6-Methyl-2-pyridinemethanol).
6-Methyl-2-pyridinemethanol (cas: 1122-71-0) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Safety of 6-Methyl-2-pyridinemethanol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts