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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 660823생성일: 2026년 10월 26일

Sodium hydride → [(2-Benzyloxy-4-chlorophenyl)-tert-butoxycarbonylamino]-acetic Acid Methyl Ester

https://huagongshe.com/reaction/660823

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Methyl bromoacetateHCID 60984—
반응물2-benzyloxy-4-chloro-N-tert-butoxycarbonylanilineHCID 22010963—
용매DimethylformamideHCID 6228—
생성물[(2-Benzyloxy-4-chlorophenyl)-tert-butoxycarbonylamino]-acetic Acid Methyl EsterHCID 68838982—

반응 조건

온도0 °C

반응 단계

To a solution of (2-benzyloxy-4-chlorophenyl)-carbamic acid tert-butyl ester (14.75 g, 44.2 mmol) in DMF (150 mL) at 0° C. is added NaH (1.94 g, 60% in mineral oil, 48.6 mmol) and the mixture is stirred at 0° C. for 10 min. To this is added methyl bromoacetate (5.04 mL, 53 mmol) and the mixture is stirred at RT for 8 h. The mixture is poured into ice/water (150 mL) and is extracted with EtOAc (700 mL). The organic phase is washed with 1N HCl (3×150 mL) and brine (150 mL) then is dried over sodium sulfate. The solvent is removed under reduced pressure and the residue purified by flash chromatography using a gradient of 5-10% EtOAc/hexane as eluent to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08084448B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-341a173e958040c1b86804bbf24b6716
출처 메모uspto-grants-2011_12