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HRID 447774作成日:2026年10月25日

4-Bromo-2,6-difluoroaniline → 5-Bromo-1,3-difluoro-2-nitrobenzene

https://huagongshe.com/reaction/447774

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromo-2,6-difluoroanilineHCID 610191—
反応物Sodium;3-oxidodioxaborirane;tetrahydrateHCID 23693097—
溶媒Acetic AcidHCID 176—
生成物5-Bromo-1,3-difluoro-2-nitrobenzeneHCID 21335487—

反応条件

温度65 °C

反応手順

To a suspension of sodium perborate tetrahydrate (1.78 mmol, 0.27 g) in 10 ml of acetic acid stirred at 65° C. was added a solution of (4-bromo-2,6-difluorophenyl)amine (1.78 mmol, 0.42 g, 1 eq.) in 5 ml of acetic acid over one hour dropwise. The reaction was heated at 65° C. over 3 days. Sodium perborate tetrahydrate (2 eq., 3.56 mmol, 0.54 g) was added again. After 3 hours, sodium perborate tetrahydrate (1 eq., 1.78 mmol, 0.27 g) was added again. Additional sodium perborate tetrahydrate (3 eq., 5.34 mmol, 0.81 g) was again added. The reaction was then left overnight at 70° C. under reflux and under argon. The solution was then cooled to room temperature and poured onto ice and extracted with ethyl acetate (2×). The combined organics were washed with water and brine. The organics were dried over MgSO4, filtered and the organic solvent was removed under reduced pressure to afford the crude product which was purified by silica chromatography (ethyl acetate-4% n-hexane 96%) to afford the title compound, 0.29 g, 68%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481566B2
出典データセットuspto-grants-2013_07
ORD IDord-946d62b7c6954c9d83b9f85c44c5ef13
出典メモuspto-grants-2013_07