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HRID 29264作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/29264

反応式

関与物質

役割名称HCID仕込み量
反応物1-(2-Bromo-4-fluorophenyl)ethan-1-oneHCID 2736304—
反応物Phenyltrimethylammonium bromide dibromideHCID 17977687—
溶媒TetrahydrofuranHCID 8028—
生成物2-Bromo-1-(2-bromo-4-fluorophenyl)ethanoneHCID 2186494863%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420066B2
出典データセットuspto-grants-2008_09
ORD IDord-56e3fb3e9d4345ee8837a0387bd56cf1
出典メモuspto-grants-2008_09