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HRID 1468765作成日:2026年10月25日

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

https://huagongshe.com/reaction/1468765

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
反応物6-Bromo-1,4-dihydro-2H-3,1-benzoxazin-2-oneHCID 25918963—
溶媒DimethylformamideHCID 6228—
生成物6-bromo-1-{[2-(trimethylsilyl)ethoxy]methyl}-1,4-dihydro-2H-3,1-benzoxazin-2-oneHCID 6797766085.4%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09006232B2
出典データセットuspto-grants-2015_04
ORD IDord-0f78bfe11bc6498e94617a705081500e
出典メモuspto-grants-2015_04