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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169330Generated: November 2, 2026

(2-Aminoethoxy)(tert-butyl)dimethylsilane → N-[2-[tert-butyl(dimethyl)silyl]oxyethyl]oxetan-3-amine

https://huagongshe.com/reaction/2169330

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Aminoethoxy)(tert-butyl)dimethylsilaneHCID 529218—
Reactant3-OxetanoneHCID 15024254—
SolventMethanolHCID 887—
ProductN-[2-[tert-butyl(dimethyl)silyl]oxyethyl]oxetan-3-amineHCID 86725969249.3%

Reaction Steps

To a stirred solution of oxetan-3-one (1 g, 13.87 mmol) in methanol (40 mL) was added 2-(tert-butyl-dimethylsilanyloxy)-ethylamine (2.7 mg, 15.27 mmol). The mixture was stirred for 30 min at room temperature after cooling, Na(CN)BH3 was added portion-wise, followed by stirring at room temperature for 2 h. The reaction mixture was quenched with water, extracted with dichloromethane (3×30 mL). The organic part was concentrated, dried and purified by Combi-Flash column (eluted at 20-50% ethyl acetate in hexane) to get [2-(tert-butyl-dimethylsilanyloxy)-ethyl]-oxetan-3-yl-amine (8 g) (1.5 g, 46.71%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-985b792acda3451aacc14d5d2cc19991
Source noteuspto-grants-2015_06