HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323811Generated: October 31, 2026
Water → Diethyl 2-acetamido-2-{2-[4-(1-oxo-5-phenylpentyl)phenyl]ethyl}malonate
https://huagongshe.com/reaction/323811
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 1-[4-(2-Iodoethyl)phenyl]-5-phenylpentan-1-one | HCID 22178484 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diethyl 2-acetamido-2-{2-[4-(1-oxo-5-phenylpentyl)phenyl]ethyl}malonate | HCID 22178485 | 61.1% |
Reaction Steps
A solution of diethyl 2-acetamidomalonate (30.6 g), sodium ethoxide (7.6 g) and molecular sieves 3A (5.5 g) in ethanol (80 ml) was stirred at room temperature for 20 hours. A solution of 1-[4-(2-iodoethyl)phenyl]-5-phenylpentan-1-one (18.4 g) in tetrahydrofuran (60 ml) was added thereto over 10 minutes and the mixture was refluxed under heating for 15 hours. The reaction mixture was poured into water (200 ml) and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and the solvent was distilled away under reduced pressure to give a brown oily substance (40 g). The obtained brown oily substance was purified by silica gel column chromatography (eluent; hexane: ethyl acetate=2:1) to give diethyl 2-acetamido-2-{2-[4-(1-oxo-5-phenylpentyl)phenyl]ethyl}malonate (13.8 g) as a pale yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06214873B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-d9e8b78b00d04e52948859c9240bfaf1 |
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| Source note | uspto-grants-2001_04 |
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