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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 406548생성일: 2026년 10월 24일

Ethyl Acetate → Methyl 2-[(tert-butoxycarbonyl)amino]-4-(4-chlorophenyl)-5-oxohexanoate

https://huagongshe.com/ko/reaction/406548

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Cesium carbonateHCID 10796—
반응물1-(p-Chlorophenyl)acetoneHCID 79699—
반응물methyl (2R)-2-(((tert-butoxy)carbonyl)amino)-3-iodopropanoateHCID 10903591—
용매DimethylformamideHCID 6228—
생성물Methyl 2-[(tert-butoxycarbonyl)amino]-4-(4-chlorophenyl)-5-oxohexanoateHCID 68747752—

반응 단계

To a solution of methyl N-(tert-butoxycarbonyl)-3-iodo-L-alaninate (215 g, 652 mmol) and 4-chlorophenylacetone (100 g, 593 mmol) in N,N-dimethylformamide (1.5 L) was added cesium carbonate (483 g, 1.48 mol) at room temperature. After 4 h, the mixture was then added to a stirring solution of pH 7 buffer and EtOAc. The aqueous layer was extracted with EtOAc and the combined organics were washed with pH 7 buffer, dried over sodium sulfate, filtered and concentrated. The crude product was purified by silica gel chromatography (10% ethyl acetate/heptane→30% ethyl acetate/heptane) to provide the title compound as a mixture of diastereomers. MS: m/z=392.1 (M+Na).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754096B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-949ae7fe63644f1aadca66be008f3e8a
출처 메모uspto-grants-2014_06