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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725659Generated: October 26, 2026

Acetyl chloride → n-Acetyl-4-(2-tert-butoxycarbonylaminoethyl)-piperidine

https://huagongshe.com/reaction/725659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant4-(2-Aminoethyl)piperidine, 4-BOC protectedHCID 1501849—
SolventDichloromethaneHCID 6344—
Productn-Acetyl-4-(2-tert-butoxycarbonylaminoethyl)-piperidineHCID 21458620—

Reaction Steps

0.5 g of 4-(2-tert-butoxycarbonylaminoethyl)-piperidine and 0.61 ml of triethylamine are dissolved in 5 ml of dichloromethane and, at 0° C., 0.22 ml of acetyl chloride is added. The reaction mixture is stirred at room temperature for 7 hours and then washed with water. The organic phase is concentrated by evaporation and purified by FC (10 g of silica gel, ethyl acetate/methanol=9:1). The title compound is obtained: Rf (ethyl acetate/methanol=9:1)=0.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705658
Source datasetuspto-grants-1998_01
ORD IDord-1e0dad00f5eb4065a2020491b3ae2166
Source noteuspto-grants-1998_01