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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1292655Erstellt: 25. Oktober 2026

Acetamidomalonic acid diethyl ester → 2-(Acetylamino)-2-[4-(acetyloxy)butyl]propanedioic acid, diethyl ester

https://huagongshe.com/reaction/1292655

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetamidomalonic acid diethyl esterHCID 14041—
EduktSodium hydrideHCID 24758—
Edukt1-Butanol, 4-bromo-, 1-acetateHCID 78491—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(Acetylamino)-2-[4-(acetyloxy)butyl]propanedioic acid, diethyl esterHCID 1054448498,3%

Reaktionsbedingungen

Temperatur0 °C

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 acetamido-malonate (500 g, 2.302 mol) in anhydrous dimethyl-formamide (1.2 1) 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05756832
Quelldatensatzuspto-grants-1998_05
ORD IDord-f4cda646ffb84b4aac2cccecccf68544
Quellennotizuspto-grants-1998_05