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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1717682생성일: 2026년 10월 25일

1-(2-Bromo-4-fluorophenyl)ethan-1-one → 2-Bromo-1-(2-bromo-4-fluorophenyl)ethanone

https://huagongshe.com/reaction/1717682

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Bromo-4-fluorophenyl)ethan-1-oneHCID 2736304—
반응물Phenyltrimethylammonium bromide dibromideHCID 17977687—
용매TetrahydrofuranHCID 8028—
생성물2-Bromo-1-(2-bromo-4-fluorophenyl)ethanoneHCID 2186494863%

반응 단계

To 1-(2-Bromo-4-fluoro-phenyl)ethanone (2.5 g, 11.52 mmol) in anhydrous tetrahydrofuran (53 mL) under argon was added phenyltrimethylammonium tribromide (4.33 g, 11.52 mmol, 1.0 eq) at 0° C. The reaction mixture was stirred at ambient temperature for 16 h, concentrated, and re-dissolved in ethyl acetate. The organic layer was washed with water (2×150 mL) and brine (1×100 mL), dried (MgSO4), filtered, and evaporated in vacuo. Purification using MPLC chromatography (Biotage) gave 2.14 g (63%) of 2-bromo-1-(2-bromo-4-fluoro-phenyl)-ethanone as a clear oil. 1H-NMR (CD2Cl2) δ 7.57 (dd, J=9.6 Hz, 1H), 7.44 (dd, J=8, 2 Hz, 1H), 7.21 (m, 7.21-7.14, 1H), 4.51 (s, 2H); TLC Rf=0.38, 15% ethyl acetate-hexanes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07803956B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-09b2551de25048afad84390ed8512051
출처 메모uspto-grants-2010_09