HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901718Generated: October 26, 2026
4-Hydroxybiphenyl → 4-(4-Nitrophenoxy)-1,1'-biphenyl
https://huagongshe.com/reaction/901718
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybiphenyl | HCID 7103 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Nitrophenoxy)-1,1'-biphenyl | HCID 240864 | — |
Reaction Steps
To a stirred solution of 1-fluoro-4-nitrobenzene (10 mmol) in DMF (20 mL) at room temperature, solid K2CO3 (30 mmol) was added followed by addition of 4-hydroxybiphenyl (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 room temperature to room temperature, the reaction mixture was poured into EtOAc (100 mL), washed with water (2×50 mL) and brine (50 mL), and dried over sodium sulfate. The solvent was removed in vacuo to afford the desired 4-(biphenyl-4-oxy)-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-408c748ba3904334a2f6325671b6b53d |
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| Source note | uspto-grants-2008_04 |
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