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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80948생성일: 2026년 10월 25일

Dichloromethane → 5-{[(S)-1-(4-Chloro-phenyl)-ethyl]-methoxycarbonyl-amino}-3-hydroxy-3-phenyl-pentanoic acid methyl ester

https://huagongshe.com/reaction/80948

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Methyl bromoacetateHCID 60984—
반응물[(S)-1-(4-Chloro-phenyl)-ethyl]-(3-oxo-3-phenyl-propyl)-carbamic acid methyl esterHCID 58109487—
반응물HCID 178418750HCID 178418750—
용매1,2-DichloroethaneHCID 11—
생성물5-{[(S)-1-(4-Chloro-phenyl)-ethyl]-methoxycarbonyl-amino}-3-hydroxy-3-phenyl-pentanoic acid methyl esterHCID 58109147—

반응 조건

온도0 °C

반응 단계

Et2Zn (1 M in hexane, 55 mL) was added dropwise to [(S)-1-(4-chloro-phenyl)-ethyl]-(3-oxo-3-phenyl-propyl)-carbamic acid methyl ester (3.80 g) dissolved in 1,2-dichloroethane (30 mL) and chilled to 0° C. under argon atmosphere. Then, (Ph3P)3RhCl (0.50 g) was added followed by the dropwise addition of methyl bromoacetate (1.0 mL) dissolved in 1,2-dichloroethane (10 mL). The resulting solution was stirred at 0-5° C. for 1 h and at ambient temperature for another 1.5 h. The solution was poured into ice-cold half-saturated aqueous NH4Cl solution (150 mL). After addition of dichloromethane, the mixture was filtered through Celite which was extracted with an additional portion of dichloromethane. The organic phase was separated and washed with water and dried (MgSO4). The solvent was removed and the residue was purified by chromatography on silica gel (cyclohexane/ethyl acetate 85:15→70:30) to give the title compound as a mixture of two diastereomers.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846668B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4f1f5b5f923146a896558a29ef35e86c
출처 메모uspto-grants-2014_09