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HRID 1468765생성일: 2026년 10월 26일

Sodium hydride → 6-bromo-1-{[2-(trimethylsilyl)ethoxy]methyl}-1,4-dihydro-2H-3,1-benzoxazin-2-one

https://huagongshe.com/reaction/1468765

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
반응물6-Bromo-1,4-dihydro-2H-3,1-benzoxazin-2-oneHCID 25918963—
용매DimethylformamideHCID 6228—
생성물6-bromo-1-{[2-(trimethylsilyl)ethoxy]methyl}-1,4-dihydro-2H-3,1-benzoxazin-2-oneHCID 6797766085.4%

반응 단계

To a solution of sodium hydride (55 wt % in mineral oil, 1.36 g, 31.2 mmol) in N,N-dimethylformamide (37 ml) was added 6-bromo-1,4-dihydro-2H-3,1-benzoxazin-2-one (5.93 g, 26.0 mmol) in N,N-dimethylformamide (37 ml) at 0° C. The mixture was stirred at room temperature for one hour, then 2-(chloromethoxy)ethyltrimethylsilane (4.77 g, 28.6 mmol) was added at 0° C. The mixture was stirred at room temperature overnight. The mixture was partitioned between water and ethyl acetate. The organic layer was washed with water (four times), dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography (eluent; hexane/ethyl acetate=90/10 to 60/40) to afford 6-bromo-1-{[2-(trimethylsilyl)ethoxy]methyl}-1,4-dihydro-2H-3,1-benzoxazin-2-one as a pale yellow solid (7.96 g, 22.2 mmol, 85%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006232B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-0f78bfe11bc6498e94617a705081500e
출처 메모uspto-grants-2015_04