HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484971Generated: October 29, 2026
Ethylenediamine → 1-Benzyl-3-oxopiperazine
https://huagongshe.com/reaction/484971
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Benzyl-3-oxopiperazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04534897 |
|---|
| Source dataset | uspto-grants-1985_08 |
|---|
| ORD ID | ord-e8ab0f488ff54d469f520da04f5d3790 |
|---|
| Source note | uspto-grants-1985_08 |
|---|