HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853812Generated: October 30, 2026
Phenacyl bromide → Diethyl acetamido(2-oxo-2-phenylethyl)propanedioate
https://huagongshe.com/reaction/853812
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl acetamido(2-oxo-2-phenylethyl)propanedioate | HCID 233989 | — |
Reaction Steps
Sodium hydride (15 mmol) is added to anhydrous ethanol (50 mL) and to the resulting sodium ethoxide solution is added 2-acetylaminomalonic acid diethyl ester (15 mmol) in one portion. The resulting mixture is stirred at room temperature for 30 minutes. A solution of 2-bromoacetophenone (10 mmol) in ethanol (10 mL) is then added and the resulting mixture is stirred at room temperature for 12 hours. After concentrating under reduced pressure, the residue is dissolved in EtOAc and water. The organic phase is washed with brine and dried over Na2SO4. After removal of the solvent, the crude material is purified by column chromatography using EtOAc/hexane (1/3) giving 2-acetylamino-2-(2-oxo-2-phenyl-ethyl)-malonic acid diethyl ester as white solid; MS: (ES+): 336.1 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07256206B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-6fa26508b22e43b5aa871bebd335a2ba |
|---|
| Source note | uspto-grants-2007_08 |
|---|