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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420852Generated: October 30, 2026

Triethylamine → Benzyl 4-(2-aminoethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/420852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAminoethylpiperazineHCID 8795—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 4-(2-aminoethyl)piperazine-1-carboxylateHCID 10890711—

Reaction Steps

N-(2-Aminoethyl)piperazine (4.93 g) was dissolved in tetrahydrofuran (40 ml), and the solution was added with triethylamine (10.6 ml). The mixture was added with a solution of benzyl chloroformate (4.9 ml) in tetrahydrofuran (40 ml) under ice cooling, and the mixture was stirred at room temperature for 1 hour. The reaction mixture was added with ethyl acetate and saturated aqueous sodium hydrogencarbonate, the layers were separated, and then the organic layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (chloroform:methanol:28% aqueous ammonia=10:1:0.1) to obtain the title compound (400 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097708B2
Source datasetuspto-grants-2012_01
ORD IDord-bdfe9dff823441fb8f66da1da7645455
Source noteuspto-grants-2012_01