HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110873Generated: October 25, 2026
N-(4-fluorophenyl)acetamide → 4-Fluoro-N-(4-fluorophenyl)benzenamine
https://huagongshe.com/reaction/1110873
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-(4-fluorophenyl)acetamide | HCID 9601 | — |
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 4-Fluoro-N-(4-fluorophenyl)benzenamine | HCID 11241173 | — |
Reaction Steps
A mixture of p-fluoroacetanilide (76.5 g, 0.5 mole), 4-bromofluorobenzene (262.5 g, 1.5 mole), K2CO3 (76 g, 0.55 mole), Cu2Br2 (157.8 g, 0.55 mole) and N-methylpyrrolidone (600 ml) were heated at 175°-180°. After allowing low boiling material to condense off, the mixture was heated at reflux for 7 days. The mixture was cooled to 60° and quenched into a mixture of 2 liters H2O, 600 ml ethylenediamine and 1.2 liters toluene, filtered and the toluene layer separated, back-washed 2×600 ml H2O, treated with activated carbon, dried over MgSO4 and concentrated to oily solids in vacuo. The latter were taken up in 1.5 liters 10% ethanolic KOH, refluxed 18 hours and concentrated in vacuo to an oil. The oil was partitioned between 750 ml H2O and 750 ml. ether. The water layer was washed 2× 200 ml ether. The organic layers were combined, back-washed 2×200 ml H2O, treated with activated carbon, dried over MgSO4, reconcentrated to an oil (60.3 g) and distilled to yield purified title product 41.6 g, b.p. 158°-160°/2 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04977178 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-f9dc723aef814a3e850277ccea2b1499 |
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| Source note | uspto-grants-1990_12 |
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