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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(1,1'-Biphenyl)-4-yl-2-bromoethanone | HCID 67282 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69428762 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07169817B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-209e9ee0f2214519a2c2673294153c11 |
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| Source note | uspto-grants-2007_01 |
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