HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Bromo-2-nitrophenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Bromophenol | HCID 11563 | — |
| Reactant | Sodium Nitrate | HCID 24268 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Bromo-2-nitrophenol | HCID 13970496 | 20% |
Reaction Steps
3-Bromophenol (32.9 g, 0.19 mol) was added slowly to a cold (10° C.) solution of sodium nitrate (29.0 g, 0.34 mol) in conc. sulfuric acid; (40.0 g) and water (70.0 mL) and the resulting mixture was allowed to stir at room temperature for 2 h. Water (200 mL) was added and the resulting mixture was extracted with diethyl ether and the extract was dried (MgSO4), filtered and concentrated. The residue was purified by flash chromatography (silica gel, 10% ethyl acetate/hexanes) to afford first the title compound (8.1 g, 20%), mp 40–42° C., then the undesired isomer, 3-bromo-4-nitrophenol, as a yellow solid (12.7 g, 31%). mp 125–127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07160870B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-cee6bd3b80874717b72564e7068394bd |
| Source note | uspto-grants-2007_01 |