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HRID 29881作成日:2026年10月27日

4-Fluorophenol → 3-(4-Fluorophenoxy)aniline

https://huagongshe.com/reaction/29881

反応式

関与物質

役割名称HCID仕込み量
反応物4-FluorophenolHCID 9732—
反応物1-Fluoro-3-nitrobenzeneHCID 9823—
反応物Potassium CarbonateHCID 11430—
溶媒DimethylamineHCID 674—
生成物3-(4-Fluorophenoxy)anilineHCID 2350601591.2%

反応手順

Alternatively, 3-(4-fluoro-phenoxy)-phenylamine was prepared by a two-step procedure by heating a suspension of m-fluoronitrobenzene (4.06 g, 28.7 mmol), p-fluorophenol (3.21 g, 28.6 mmol) and K2CO3 (8.13 g, 58.8 mmol) in DMA (dimethylamine) (60 mL) at 150° C. for 3 hours. The brown reaction mixture was concentrated to one-quarter original volume, diluted with ethyl acetate (220 mL) and washed successively with water (220 mL), 1N NaOH (220 mL) and brine (220 mL). The organic layer was dried (MgSO4) and the solvent removed in vacuo to afford the diphenylether (5.30 g, 80%) as a brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423043B2
出典データセットuspto-grants-2008_09
ORD IDord-2b2c63fa300748dea9d913c55c851a3d
出典メモuspto-grants-2008_09