HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Piperidineethanol | HCID 73953 | — |
| Reactant | Tert-butyldicarbonate | HCID 22064466 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidine | HCID 854140 | 100% |
Reaction Steps
To a solution of 4-piperidine ethanol (1.95 g) in acetonitrile (25 mL) was added triethylamine (2.53 mL) followed by tert-butyl dicarbonate (3.63 g). The mixture was stirred at room temperature for 22 hours and partitioned between 0.5 M hydrochloric acid and ethyl acetate. The organic layer was washed with brine, dried (MgSO4) and the solvent evaporated to give 4-(2-hydroxy-ethyl)-piperidine-1-carboxylic acid tert-butyl ester (3.46 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08252792B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-79e18e7ed1ad46029ede010052f5f2cf |
| Source note | uspto-grants-2012_08 |