Some low molecular weight alcohols of industrial importance are produced by the addition of water to alkenes. 7748-36-9, formula is C3H6O2, Ethanol, isopropanol, 2-butanol, and tert-butanol are produced by this general method. Two implementations are employed, the direct and indirect methods. Synthetic Route of 7748-36-9
Wang, Xueqin;Xu, Ruiqiu;Zhang, Pang research published 《 Synthesis of 3-hydroxyoxetane and the Finkelstein reaction of its p-toluenesulfonate with sodium iodide》, the research content is summarized as follows. Successive tosylation and benzoylation of HOCH2CH(OCH2Ph)CH2OH gave PhCO2CH2CH(OCH2Ph)CH2OTs (Ts = p-tosyl), which was cyclized with MeONa in boiling MeOH to give I (R = PhCH2) (II) in 30% overall yield. Catalytic hydrogenolysis of II gave 90% title compound (I; R = H), which was tosylated to give 86% I (R = Ts) (III). III underwent a slower Finkelstein reaction with NaI than 1,3-di-O-methylglycerol p-tosylate due to the electron-withdrawing inductive effect of the ring O atom.
Synthetic Route of 7748-36-9, Oxetan-3-ol is a useful research compound. Its molecular formula is C3H6O2 and its molecular weight is 74.08 g/mol. The purity is usually 95%.
Oxetan-3-ol is a synthetic hydroxy compound with the chemical formula C6H12O3. It is an organic solvent that can be used in reactions involving vinyl alcohol and oxetane, such as ring-opening polymerization and cationic polymerization. Oxetan-3-ol has also been shown to react with ethyl bromoacetate to form the corresponding oxetane, which can be used as a bioisostere for chloropropane, a potential replacement for chlorofluorocarbons., 7748-36-9.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts