HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 52812Erstellt: 24. Oktober 2026
Acetamidomalonic acid diethyl ester → HCID 10544484, Verbindung
https://huagongshe.com/de/reaction/52812
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 1-Butanol, 4-bromo-, 1-acetate | HCID 78491 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 10544484 | HCID 10544484 | 98,3% |
Reaktionsschritte
A stirred suspension of 95% sodium hydride (60.8 g, 2.532 mol) in anhydrous dimethylformamide (500 ml) under an atmosphere of argon was cooled to 0° C. (ice bath). A solution of diethyl acetamidomalonate (500 g, 2.302 mol) in anhydrous dimethylformamide (1.2 l) was added over a period of 45 minutes while keeping the reaction temperature below 18° C. After the addition was complete, the turbid solution was gradually warmed to room temperature. After stirring for one hour at room temperature, 4-bromobutyl acetate (471.5 g, 2.417 mol) was added. The mixture was then stirred at 59°-60° C. for 18 hours. The resulting slurry was cooled to room temperature, quenched with absolute ethanol (40 ml) and glacial acetic acid (4 ml), stirred for about 15 minutes, poured into a 10% lithium chloride solution and extracted with ethyl acetate (2×3 l). The combined ethyl acetate extracts were washed with 10% lithium chloride (3×3 l), dried (anhydrous sodium sulfate), and evaporated in vacuo to give 750 g of title product as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05616775 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-c18b93b4b3584bbda3629d1892b74815 |
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| Quellennotiz | uspto-grants-1997_04 |
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