HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Tert-butyl-dimethyl-(3-piperidylmethoxy)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Piperidin-3-ylmethanol | HCID 107308 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl-dimethyl-(3-piperidylmethoxy)silane | HCID 58992622 | 60.5% |
Reaction Steps
To a solution of piperidin-3-ylmethanol (2.10 g, 0.018 mol) in CH2Cl2 (20 mL) is added triethylamine (5.53 g, 0.0547 mol) followed by t-butyldimethylchlorosilane (4.127 g, 0.0275 mol) and the reaction mixture is stirred at room temperature. After 24 hours, the reaction mixture is washed with water, saturated solution of NaHCO3, and brine. The combined organic layers are combined and dried over sodium sulfate, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (silica gel) over a gradient using 0-10% MeOH in dichloromethane to afford the title compound (2.50 g, 60%). Mass spectrum (m/z): 231.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642768B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-09e2d7e51851416abe4c0165466b7282 |
| Source note | uspto-grants-2014_02 |