HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17719Generated: October 25, 2026
Water → 4-(Dibenzofuran-2-yloxy)-1-nitrobenzene
https://huagongshe.com/reaction/17719
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Dibenzofuranol | HCID 66587 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Dibenzofuran-2-yloxy)-1-nitrobenzene | HCID 2102893 | — |
Reaction Steps
To a stirred solution of 1-fluoro-4-nitrobenzene (10 mmol) in DMF (20 mL) at rt, solid potassium carbonate (30 mmol) was added followed by addition of 2-hydroxydibenzofuran (10 mmol) to the reaction mixture and heating to 80° C. until the reaction was complete as indicated by TLC or HPLC. After cooling to rt, the reaction mixture was poured into H2O (100 mL), extracted with EtOAc (2×50 mL), washed with H2O (2×50 mL) and brine (50 mL), and dried over sodium sulfate. The solvent was removed in vacuuo to afford the desired 4-(dibenzofuran-2-yloxy)-1-nitrobenzene. The crude product was used for further transformation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737285B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-ea8a6170526e4f7d827a200b6cabdcc3 |
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| Source note | uspto-grants-2010_06 |
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