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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395250Generated: November 4, 2026

Acetic Anhydride → N-Ethyl-2-(piperidin-1-yl)ethan-1-amine

https://huagongshe.com/reaction/2395250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantN-(2-Aminoethyl)piperidineHCID 33944—
SolventDichloromethaneHCID 6344—
ProductN-Ethyl-2-(piperidin-1-yl)ethan-1-amineHCID 1875300779%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05814634
Source datasetuspto-grants-1998_09
ORD IDord-6cb8a8411d704825b480ef9b8c3f7f7f
Source noteuspto-grants-1998_09