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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7536생성일: 2026년 10월 23일

Pyridine → Ethyl 3-acetamido-2-oxopentanoate

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

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Ethoxalyl chlorideHCID 20884—
반응물2-(Acetylamino)butanoic acidHCID 306107—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 3-acetamido-2-oxopentanoateHCID 21935058—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087605B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-104f1562f4d446dfad9da36770411e4b
출처 메모uspto-grants-2006_08