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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375917Generated: November 1, 2026

Acetamidomalonic acid diethyl ester → HCID 69428762, compound

https://huagongshe.com/reaction/1375917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidomalonic acid diethyl esterHCID 14041—
ReactantSodium hydrideHCID 24758—
Reactant1-(1,1'-Biphenyl)-4-yl-2-bromoethanoneHCID 67282—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductHCID 69428762HCID 69428762—

Reaction Steps

Sodium hydride (15 mmol) is added to anhydrous ethanol (50 mL). To this 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 min. A solution of 4′-phenyl-2-bromoacetophenone (10 mmol) in ethanol (10 mL) is then added and the resulting mixture is stirred at room temperature for 12 h. 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 the desired product as white solid. 1H NMR (400 MHz, CDCl3) δ 8.03 (d, J=8.6 Hz, 2H), 7.68 (d, J=8.6 Hz, 2H), 7.61 (d, J=8.5 Hz, 2H), 7.45 (m, 3H), 7.13 (s, 1H), 4.28 (m, 6H), 1.98 (s, 2H), 1.26 (t, J=7.1 Hz, 6H); MS: (ES+): 412.2 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169817B2
Source datasetuspto-grants-2007_01
ORD IDord-209e9ee0f2214519a2c2673294153c11
Source noteuspto-grants-2007_01