HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17669Generated: October 25, 2026
Water → 1-Fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzene
https://huagongshe.com/reaction/17669
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluoro-3-(trifluoromethyl)phenol | HCID 601854 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzene | HCID 66977640 | — |
Reaction Steps
To a stirred solution of 4-fluoronitrobenzene (20 mmol), 4-fluoro-3-trifluoromethylphenol (22 mmol) in DMF (50 mL) at rt, solid potassium carbonate (60 mmol) was added, and the reaction mixture was heated to 90° C. for 5 h (monitored by TLC), according to General Procedure L1. After cooling to rt, the reaction mixture was poured into cold H2O (60 mL). The resulting mixture was extracted with EtOAc (3×100 mL). The combined EtOAc extracts were washed with H2O (2×40 mL) and brine (50 mL), and dried over anhydrous sodium sulfate. The solvent was removed in vacuuo to afford the desired 1-fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzene. The crude product was used directly for further transformation without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07737285B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-e8b78f2aa3ee4ad4b060986ede17fb87 |
|---|
| Source note | uspto-grants-2010_06 |
|---|