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HRID 495800作成日:2026年10月26日

Ethanol → Ethyl 2-((tert-butoxycarbonyl)amino)acetate

https://huagongshe.com/reaction/495800

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物N-(tert-butoxycarbonyl)glycineHCID 78288—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium BisulfateHCID 516919—
生成物Ethyl 2-((tert-butoxycarbonyl)amino)acetateHCID 35772991.7%

反応条件

温度0 °C

反応手順

(tert-Butoxycarbonylamino)acetic acid (4.00 g, 22.8 mmol) was dissolved in dichloromethane (8 ml). Ethanol (1.60 ml, 27.40 mmol) and 4-dimethylaminopyridine (0.31 g, 25.1 mmol) were added. The solution was cooled to 0° C. N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (4.81 g, 25.11 mmol) was added. The solution was stirred for 16 h, while warming up to room temperature. It was diluted with ethyl acetate (150 ml) and 10% aqueous sodium hydrogen sulfate solution (100 ml). The phases were separated. The aqueous phase was extracted with ethyl acetate (4×50 ml). The combined organic layers were washed with saturated sodium hydrogen carbonate solution (150 ml) and dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (100 g), using ethyl acetate/heptane (1:4) as eluent, to give 4.25 g of ethyl 2-(tert-butoxycarbonylamino)acetate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06939880B2
出典データセットuspto-grants-2005_09
ORD IDord-90582ce327074410882fb9b84df6a20b
出典メモuspto-grants-2005_09