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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383752Generated: October 29, 2026

Potassium Iodide → Ethyl (2-carbamoylmethoxyethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1383752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-Piperazinecarboxylic acid, ethyl esterHCID 8431—
ReactantSodium CarbonateHCID 10340—
Reactant2-(2-Chloroethoxy)acetamideHCID 11018931—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventIsopropanolHCID 3776—
ProductEthyl (2-carbamoylmethoxyethyl)piperazine-1-carboxylateHCID 5380365281.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

164 g (1.04 mol) of ethyl piperazinecarboxylate, 156.9 g (1.14 mol) of (2-chloroethoxy)acetamide, 241.7 g (2.28 mol) of sodium carbonate, 1g of potassium iodide and 200 ml of toluene are introduced into a 2 l three-necked round-bottomed flask fitted with a water-cooled condenser and a mechanical stirrer. The mixture is brought at the reflux temperature for 3 hours 30. The mixture is allowed to cool to 50° C., and 200 ml of isopropanol are added. The reaction mixture is filtered and the filtration residue is washed with 150 ml of isopropanol. The filtrate is concentrated on a rotary evaporator under reduced pressure. 277.2 g of crude product are obtained, which product is recrystallized from 500 ml of ethyl acetate. 219.2 g (81.6%) of ethyl (2-carbamoylmethoxyethyl)piperazine-1-carboxylate are obtained in the form of a white solid. NMR: δ: 1.24 (3H, t, 7.05 Hz); 2.46 (4H, m); 2.57 (2H, t, 5.2 Hz); 3.44 (4H, m); 3.62 (2H, t, 5.2 Hz); 3.95 (2H, s); 4.1 (2H, 9, 7.1 Hz); 5.72 (1H, bs); 7.34 (1H, bs). Mass spectrum: 260 (MH+). DSC: Onset 106.5° C., Max: 109.7° C. Elemental analysis:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255487B1
Source datasetuspto-grants-2001_07
ORD IDord-8ac7a9df8a5d4e929cf9d18ed008b11d
Source noteuspto-grants-2001_07