HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Aminoethoxy)(tert-butyl)dimethylsilane → N-[2-[tert-butyl(dimethyl)silyl]oxyethyl]oxetan-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Aminoethoxy)(tert-butyl)dimethylsilane | HCID 529218 | — |
| Reactant | 3-Oxetanone | HCID 15024254 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-[2-[tert-butyl(dimethyl)silyl]oxyethyl]oxetan-3-amine | HCID 86725969 | 249.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045486B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-985b792acda3451aacc14d5d2cc19991 |
| Source note | uspto-grants-2015_06 |