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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383753Generated: October 31, 2026

Water → Ethyl 4-(2-carbamoylmethoxyethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1383753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Piperazinecarboxylic acid, ethyl esterHCID 8431—
ReactantSodium CarbonateHCID 10340—
Reactant2-(2-Chloroethoxy)acetamideHCID 11018931—
CatalystPotassium IodideHCID 4875—
SolventTolueneHCID 1140—
SolventIsopropanolHCID 3776—
ProductEthyl 4-(2-carbamoylmethoxyethyl)piperazine-1-carboxylateHCID 2118837882.3%

Reaction Steps

15.13 g of (2-chloroethoxy)acetamide (0.11 mol), 14.6 ml of ethyl piperazine carboxylate (0.1 mol), 23.3 g of sodium carbonate (0.22 mol) and 1.0 g of potassium iodide in 25 ml of toluene are introduced into a round-bottomed flask fitted with a water-cooled condenser and a mechanical stirrer. The mixture is heated at the reflux temperature for 4 hours and is allowed to cool to room temperature. The reaction is continued, still with stirring, for a further 16 hours. 100 ml of isopropanol are added and the solid materials formed are filtered off. The solvent is evaporated from the filtrate under reduced pressure to dryness. The product obtained after evaporation of the solvents is recrystallized from toluene. 21.35 g of ethyl 4-(2-carbamoylmethoxyethyl)piperazine-1-carboxylate are obtained. Yield: 82%. Mass spectrum: 260 (MH+), 214 (M+−OEt).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255487B1
Source datasetuspto-grants-2001_07
ORD IDord-453d91fe6e56431e8f6fb19b2bde1b77
Source noteuspto-grants-2001_07