HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622775Generated: October 26, 2026
Ethylenediamine → 3-Phenylpiperazin-2-one
https://huagongshe.com/reaction/622775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Ethyl bromophenylacetate | HCID 97780 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Phenylpiperazin-2-one | HCID 250681 | 54.3% |
Reaction Steps
To a stirred solution of 1928 g (32.1 mol) of ethylenediamine in 2 liters of absolute ethanol was added a solution of 3130 g (12.8 mol) of ethyl α-bromophenylacetate in 4 liters of absolute ethanol at such a rate so as to maintain reflux (~45 minutes addition time). The mixture was allowed to cool to ambient temperature and then concentrated to a thick yellow slurry. The slurry was stirred with 2 liters of chloroform, filtered, and the solid washed thoroughly with chloroform (total of 8 liters). The filtrate was concentrated to near dryness and the resulting residue stirred for a short time with 2 liters of isopropanol. The solid was collected by filtration, washed with 4 liters of isopropanol, and dried to give 1224 g (54%) of 3-phenyl-2-piperazinone. This material was used as such in the next step. [Pure material could be obtained by recrystallization from benzene and then from acetone to give a white solid (mp. 139.0°-139.5° C. ).]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04772705 |
|---|
| Source dataset | uspto-grants-1988_09 |
|---|
| ORD ID | ord-8e8d9d0d0f414f819662d27866224cc5 |
|---|
| Source note | uspto-grants-1988_09 |
|---|