HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237036Generated: October 25, 2026
Water → 4-(4-Methoxynaphthalen-1-yloxy)-1-nitrobenzene
https://huagongshe.com/reaction/2237036
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methoxy-1-naphthol | HCID 66542 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Methoxynaphthalen-1-yloxy)-1-nitrobenzene | HCID 66977374 | — |
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 4-methoxy-1-naphthol (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-(4-methoxynaphthalen-1-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 | US07714013B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-8da8b8f774464d739d915b89291c1ad1 |
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| Source note | uspto-grants-2010_05 |
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