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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981614Generated: November 3, 2026

Ethylenediamine → 1-Benzyl-3-oxopiperazine

https://huagongshe.com/reaction/1981614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantBenzyl ChlorideHCID 7503—
ReactantEthyl chloroacetateHCID 7751—
ReactantSodium CarbonateHCID 10340—
ReactantSodium MethoxideHCID 10942334—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
Product1-Benzyl-3-oxopiperazineHCID 11458177—

Reaction Steps

A solution of ethyl chloroacetate (204 g., 1.67 mole) in ethanol (500 ml.) is added to a stirred solution of ethylenediamine (600 g., 10 mole) in ethanol (3 l.) at 0°. After addition is complete the solution is allowed to warm to 20°-25°. After 5 hours a solution of sodium methoxide (90.0 g., 1.67 mole) in methanol (200 ml.) is added and the solution is stirred overnight, filtered to remove inorganic salts and evaporated to remove solvent and unreacted ethylenediamine. The residual oil (189 g.) is added to a mixture of benzyl chloride (241 g., 1.9 mole) anhydrous sodium carbonate (191 g., 2.28 mole) in ethanol (2.3 l.) and the solution is stirred under reflux for 3 hours. The ethanol is removed under reduced pressure and the residue is partitioned between chloroform and water. Evaporation of the chloroform gave a crystalline product which was recrystallized from ethyl acetate to give the title compound, m.p. 154°- 156°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04593098
Source datasetuspto-grants-1986_06
ORD IDord-bff7c02001ea4f44b8a714163afb4295
Source noteuspto-grants-1986_06