돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 588732생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/588732

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 ambient temperature 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 (500 mL) and ethyl acetate (2×200 mL). The combined organic layers were washed with brine, dried over sodium sulfate and concentrated in vacuo to give the title compound as a 1:1 racemic mixture of diastereomers, which was used without further purification. MS: m/z=314.1 (M−t-Bu+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09227972B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-2f0ad1b48fd14a2eac2dae56112ed563
출처 메모uspto-grants-2016_01