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HRID 1379330作成日:2026年10月27日

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

https://huagongshe.com/reaction/1379330

反応式

関与物質

役割名称HCID仕込み量
反応物Acetamidomalonic acid diethyl esterHCID 14041—
反応物Sodium hydrideHCID 24758—
反応物1-Butanol, 4-bromo-, 1-acetateHCID 78491—
溶媒DimethylformamideHCID 6228—
生成物2-(Acetylamino)-2-[4-(acetyloxy)butyl]propanedioic acid, diethyl esterHCID 1054448498.3%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05670699
出典データセットuspto-grants-1997_09
ORD IDord-add267fea44546a498f65080e3adc1ac
出典メモuspto-grants-1997_09