HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-Ethyl-2-(piperidin-1-yl)ethan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(2-Aminoethyl)piperidine | HCID 33944 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Ethyl-2-(piperidin-1-yl)ethan-1-amine | HCID 18753007 | 79% |
Reaction Steps
To a solution of 1-(2-aminoethyl)piperidine(5.01 g) in dichloromethane (100 ml) were added triethylamine(11 ml) and acetic anhydride(4.4 ml) and then the mixture was stirred at room temperature for 40 minutes. The reaction solution was washed with saturated sodium hydrogencarbonate aqueous solution and saturated brine successively, dried over sodium sulfate anhydride, and concentrated under a vacuum. The residue was dropped into a suspension of lithium aluminium hydride (3.46 g) in tetrahydrofuran(100 ml). After being refluxed with heating for 1 hour, the reaction mixture was filtrated. The filtrate was concentrated, thereby yielding 4.43 g(79%) of 1-[2-(ethylamino)ethyl]piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05814634 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-6cb8a8411d704825b480ef9b8c3f7f7f |
| Source note | uspto-grants-1998_09 |