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HRID 1517589생성일: 2026년 10월 26일

Acetamide → 2-((2-Bromopyridin-3-yl)oxy)acetamide

https://huagongshe.com/reaction/1517589

반응식

참여 물질

역할이름HCID투입량
반응물AcetamideHCID 178—
반응물2-Bromo-3-pyridinolHCID 23070—
반응물Sodium hydrideHCID 24758—
용매TetrahydrofuranHCID 8028—
생성물2-((2-Bromopyridin-3-yl)oxy)acetamideHCID 4780809975%

반응 단계

To a solution of 2-bromo-3-pyridinol (1.5 g, 8.49 mmol) in tetrahydrofuran (15 mL) at 0° C. is added 60% sodium hydride in mineral oil (509.44 mg, 12.74 mmol) and the mixture is stirred at that temperature for 30 min. Then acetamide, 2-chloro-(16.98 mmol) is added and the mixture is stirred at room temperature over the weekend. The mixture is quenched with water and extracted with ethyl acetate. The organic layer is separated dried on magnesium sulfate and the solvent evaporated in vacuo to give the title compound in a 75% yield. The compound is used without any further purification. MS (m/z): 231 (M+1), 233 (M+3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08232289B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-c186365d799849169d3bd529860bdbeb
출처 메모uspto-grants-2012_07