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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448224생성일: 2026년 10월 26일

Cesium carbonate → Methyl 2-[(tert-butoxycarbonyl)amino]-4-(3-chlorophenyl)-5-oxohexanoate

https://huagongshe.com/reaction/448224

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물1-(3-Chlorophenyl)propan-2-oneHCID 2734097—
반응물(S)-Methyl 2-Boc-amino-3-iodopropionateHCID 11416215—
용매DimethylformamideHCID 6228—
생성물Methyl 2-[(tert-butoxycarbonyl)amino]-4-(3-chlorophenyl)-5-oxohexanoateHCID 68750611—

반응 단계

A mixture of cesium carbonate (9.80 g, 30.1 mmol) and methyl N-(tert-butoxycarbonyl)-3-iodo-D-alaninate (9.90 g, 30.1 mmol) in DMF (75 mL) was stirred at 23° C. for 45 min before 1-(3-chlorophenyl)propan-2-one (6.09 g, 36.1 mmol) and additional cesium carbonate (9.80 g, 30.1 mmol) were added. The resulting mixture was stirred for 2.5 h. The majority of the DMF was then removed under reduced pressure at a bath temperature of <40° C. The concentrated mixture was partitioned between water (100 mL) and ethyl acetate (2×200 mL). The combined organic layers were washed with brine, dried over sodium sulfate and concentrated to give the title compound as a 1:1 racemic mixture of cis and trans diastereomers, which was used without further purification. MS: m/z=392.1 (M+Na).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481556B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-0282e4f0269240ec9243b6a49e0bd991
출처 메모uspto-grants-2013_07