HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorophenol → 3-(4-Fluorophenoxy)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | 1-Fluoro-3-nitrobenzene | HCID 9823 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylamine | HCID 674 | — |
| Product | 3-(4-Fluorophenoxy)aniline | HCID 23506015 | 91.2% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07423043B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-2b2c63fa300748dea9d913c55c851a3d |
| Source note | uspto-grants-2008_09 |