HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482727Generated: October 27, 2026
Acetamidomalonic acid diethyl ester → Diethyl acetamido[2-(2-nitrophenyl)ethyl]propanedioate
https://huagongshe.com/reaction/482727
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 2-Nitrophenethyl bromide | HCID 12363878 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl acetamido[2-(2-nitrophenyl)ethyl]propanedioate | HCID 20244794 | — |
Reaction Steps
A solution of diethyl acetamidomalonate (33.2 g) in ethanol (150 ml) was added to a solution of sodium ethoxide in ethanol [prepared from sodium (3.8 g) and ethanol (200 ml)]. The reaction mixture was stirred at room temperature for 30 minutes and a solution of 2-nitrophenethyl bromide (J. Med. Chem. 20, 1020 (1977), 40.0 g) in ethanol (100 ml) was added dropwise during 20 minutes. After addition was complete, the reaction mixture was refluxed for 18 hours, then cooled to room temperature and evaporated under reduced pressure. The residue was dissolved in water (350 ml) and the solution extracted with ethyl acetate (2×350 ml). The combined ethyl acetate extracts were washed with water (200 ml) and dried over magnesium sulfate. Removal of the solvent under reduced pressure gave diethyl 2-acetamido-2-(o-nitrophenethyl)malonate as a low melting solid, used without further purification for the next synthetic step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04575503 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-34e0cfdd8f8641408381c35d4a444ab2 |
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| Source note | uspto-grants-1986_03 |
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