HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 2-Benzyloxy-4,5-difluoronitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,5-Difluoro-2-nitrophenol | HCID 2774182 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Benzyloxy-4,5-difluoronitrobenzene | HCID 68840030 | — |
Reaction Steps
To a vigorously stirred mixture of 4,5-difluoro-2-nitrophenol (1 g, 5.71 mmol) and anhydrous potassium carbonate (1.9 g, 14.28 mmol) in acetone (20 mL). is added benzyl bromide (750 μl, 6.28 mmol) and the dark heterogeneous mixture is heated to reflux for 10 h; or until all starting material had been consumed according to LC/MS analysis. The dark mixture is then filtered, dried over magnesium sulfate, and filtered again to afford, after solvent removal, a light brown crystalline solid that was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084448B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-e27f13424c964523a059667bbc9feb36 |
| Source note | uspto-grants-2011_12 |