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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29881생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/29881

반응식

참여 물질

역할이름HCID투입량
반응물4-FluorophenolHCID 9732—
반응물1-Fluoro-3-nitrobenzeneHCID 9823—
반응물Potassium CarbonateHCID 11430—
용매DimethylamineHCID 674—
생성물3-(4-Fluorophenoxy)anilineHCID 2350601591.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423043B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-2b2c63fa300748dea9d913c55c851a3d
출처 메모uspto-grants-2008_09