HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801465Generated: October 29, 2026
Benzyl Bromide → 2-(Benzyloxy)-1-fluoro-3-nitrobenzene
https://huagongshe.com/reaction/1801465
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoro-6-nitrophenol | HCID 73710 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Benzyloxy)-1-fluoro-3-nitrobenzene | HCID 68632184 | 102.8% |
Reaction Steps
To a solution of 2-fluoro-6-nitrophenol (25.1 g, 157 mmol) in DMF (430 mL) were added K2CO3 (43.7 g, 313 mmol) and benzyl bromide (21 mL, 172 mmol). The reaction mixture was stirred at 80° C. overnight. After cooling to rt, the reaction mixture was filtered. The filtrate was concentrated under reduced pressure. Water (100 mL) and EA (100 mL) were added and the phases were separated. The aq. layer was extracted once with EA (100 mL) and the combined org. layers were dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was dried under HV to give the title compound as a yellow oil (39.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349828B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-565b562118494767a06fd37e72cbbc81 |
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| Source note | uspto-grants-2013_01 |
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