HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromo-2,5-difluoronitrobenzene → 5-Bromo-4-fluoro-2-nitrophenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromo-2,5-difluoronitrobenzene | HCID 2736286 | — |
| Reactant | Sodium trimethylsilanolate | HCID 23672319 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromo-4-fluoro-2-nitrophenol | HCID 57634114 | 205.8% |
Reaction Steps
A solution of 2 M sodium trimethylsilanolate (15.6, 31.1 mmol) in THF was added dropwise to 4-bromo-2,5-difluoronitrobenzene (2.47 g, 10.4 mmol) under a nitrogen atmosphere. A bright red suspension was formed, and the mixture was refluxed for 27 hours. The mixture was cooled to room temperature and concentrated. Water (6 mL) was added, and the solution was acidified with a 10% HCl solution, extracted with DCM (70 mL×2). The organic layers were combined and concentrated to give 5-bromo-4-fluoro-2-nitrophenol (5.05 g, 2.06%). MS m/z: 236 (M+1). 1H NMR (400 MHz, CD3OD) δ ppm 7.48 (d, J=5.87 Hz, 1H), 7.95 (d, J=8.41 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084479B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-ed676f995b4443068691f4bacd65cbcc |
| Source note | uspto-grants-2011_12 |