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HRID 2088331作成日:2026年10月24日

Tert-Butyl nitrite → 5-Ethoxy-5-oxo-4-(phenylmethoxycarbonylamino)pentanoic acid

https://huagongshe.com/ja/reaction/2088331

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-Butyl nitriteHCID 10906—
反応物2-Benzyloxycarbonylamino-4-carbamoyl-butyric acid ethyl esterHCID 14036688—
溶媒AcetonitrileHCID 6342—
生成物5-Ethoxy-5-oxo-4-(phenylmethoxycarbonylamino)pentanoic acidHCID 29242464.7%

反応手順

A suspension of the amide (2) (38 g, 0.1233 mol) in anhydrous acetonitrile (400 ml) was stirred at reflux under nitrogen and t-butyl nitrite (35 ml, 3.17 equiv.) was added quickly. The reflux was continued for 2 hrs. After cooling, the solvent was removed in a rotary evaporator. The residue was taken in water (250 ml) and ethyl acetate (500 ml) and the biphasic mixture was stirred well while solid sodium bicarbonate was slowly added to pH=7.5. Phases were separated and the organic phase was washed with 10% sodium bicarbonate (200 ml). The combined aqueous extracts were washed with ethyl acetate (300 ml), made acidic with 6N hydrochloric acid and extracted with ethyl acetate (2×300 ml). The combined extracts were washed with water (150 ml), dried over sodium sulfate, stripped and the residue was dried in a vacuum oven (50° C.) to produce (3) (24.6 g, 64.7%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08435956B2
出典データセットuspto-grants-2013_05
ORD IDord-59b04b06c6eb417cb9036f0bb6ba9836
出典メモuspto-grants-2013_05