Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Fluorophenol → 3-(4-Fluorophenoxy)aniline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Fluorophenol | HCID 9732 | — |
| 반응물 | 1-Fluoro-3-nitrobenzene | HCID 9823 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 용매 | Dimethylamine | HCID 674 | — |
| 생성물 | 3-(4-Fluorophenoxy)aniline | HCID 23506015 | 91.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07423043B2 |
| 출처 데이터셋 | uspto-grants-2008_09 |
| ORD ID | ord-2b2c63fa300748dea9d913c55c851a3d |
| 출처 메모 | uspto-grants-2008_09 |