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HRID 7536作成日:2026年10月24日

Pyridine → Ethyl 3-acetamido-2-oxopentanoate

https://huagongshe.com/ja/reaction/7536

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Ethoxalyl chlorideHCID 20884—
反応物2-(Acetylamino)butanoic acidHCID 306107—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 3-acetamido-2-oxopentanoateHCID 21935058—

反応手順

9.2 g (63.4 mmol) 2-(acetylamino)butanoic acid are suspended in 120 ml tetrahydro-furane and heated to reflux together with 15.0 g (190 mmol) pyridine and a bit of N,N-dimethylaminopyridine. While heating at reflux, 17.3 g (127 mmol) ethyl chloro(oxo)acetate are added dropwise. The reaction mixture is heated at reflux until no more evolution of gas can be observed. After cooling down to room temperature, the reaction mixture is added to ice water and the organic phase extracted with ethyl acetate. The dried organic phase is evaporated to dryness in vacuo, dissolved in ethanol and the solution directly used for the next reaction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087605B2
出典データセットuspto-grants-2006_08
ORD IDord-104f1562f4d446dfad9da36770411e4b
出典メモuspto-grants-2006_08