HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 4-(2-Fluorophenoxy)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Fluoro-2-(4-nitrophenoxy)benzene | HCID 57974999 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | 4-(2-Fluorophenoxy)aniline | HCID 5126073 | 73.4% |
Reaction Steps
Into a 250 mL 3-necked round-bottom flask, was placed a solution of 1-fluoro-2-(4-nitrophenoxy)benzene (5 g, 21.44 mmol, 1.00 equiv) in methanol/H2O (2/1=V/V) (100 mL), and NH4Cl (1 g, 18.70 mmol, 0.87 equiv). This was followed by the addition of Fe (7 g, 5.83 equiv), in portions at 80° C. in 20 min. The resulting solution was stirred for 1 h at reflux in an oil bath. The reaction mixture was cooled in a water bath. The solids were filtered out and the filtrate was concentrated under vacuum. The resulting solution was extracted with ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum to give 3.2 g (73%) of 4-(2-fluorophenoxy)aniline as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957080B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-68c6d743e32344f3a2bc4fd08c46f4ed |
| Source note | uspto-grants-2015_02 |