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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantAcetamidomalonic acid diethyl esterHCID 14041—
ReactantSodium hydrideHCID 24758—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductDiethyl acetamido(2-oxo-2-phenylethyl)propanedioateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256206B2
Source datasetuspto-grants-2007_08
ORD IDord-6fa26508b22e43b5aa871bebd335a2ba
Source noteuspto-grants-2007_08