HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Amino-1-propanol → (3-Aminopropoxy)(tert-butyl)dimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Amino-1-propanol | HCID 9086 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Aminopropoxy)(tert-butyl)dimethylsilane | HCID 11074190 | 91.6% |
Reaction Steps
A solution of 7.4 g (98 mmol) 3-aminopropanol in 10 ml THF was added at room temperature to a suspension of 4.12 sodium hydride (60%; 103.2 mmol) in 140 ml THF. The mixture was stirred for 1 hour and then 16.28 g (108 mmol) tert-butyl-dimethylsilylchloride was added and vigorous stirring was continued for 1 hour. The mixture was diluted with 300 ml diethylether and washed successively with 100 ml of aqueous K2CO3 (10%), 100 ml of water and 100 ml of brine, dried over MgSO4 and evaporated to give 17 g of light yellow crude product. This product was dissolved in ethyl acetate/hexane 1/10 and filtered through a pad of silica gel. The filtrate was concentrated in vacuo to give 13 g (70%) of the desired product as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08173609B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-93f49546213c43d6addda70c93725cf9 |
| Source note | uspto-grants-2012_05 |