HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901697Generated: October 28, 2026
Water → 4-(6-Methoxy-naphthalen-2-yloxy)-1-nitrobenzene
https://huagongshe.com/reaction/901697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Methoxy-2-naphthol | HCID 288634 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(6-Methoxy-naphthalen-2-yloxy)-1-nitrobenzene | HCID 66977464 | — |
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 6-methoxy-2-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-(6-methoxy-naphthalen-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 | US07361678B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-a00f0df7a8c246bc96998a3a6c09e836 |
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| Source note | uspto-grants-2008_04 |
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