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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937823Generated: November 1, 2026

Triethylamine → tert-Butyl 4-(2-aminoethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1937823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-ChloroethylamineHCID 13369—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-(2-aminoethyl)piperazine-1-carboxylateHCID 151440026%

Reaction Steps

A solution of N-tert-butoxycarbonyl-piperazin (5 g, 26.8 mmol), triethylamine (7.44 ml, 53.6 mmol), and chloroethylamine (3.11 g, 26.8 mmol) in dimethylformamide (50 ml) was stirred at room temperature for 72 hours. The reaction mixture was filtered, partitioned between H2O and ethyl acetate. The aqueous phase was lyophilized, the residue stirred with methanol and the precipitate collected by suction. The precipitate was purified by flash chromatography on silica gel (dichloromethane/methanol/aqueous ammonia=9/1/0.1) to give 1.6 g (26%) of the desired product. MS m/z: 230 ((M+H)+, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395737B1
Source datasetuspto-grants-2002_05
ORD IDord-f2c53517cb274bed9c83e7220f84e317
Source noteuspto-grants-2002_05