HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromohexane → 4-n-Hexyloxy-2-fluorobromobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromohexane | HCID 8101 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-3-fluorophenol | HCID 2779153 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-n-Hexyloxy-2-fluorobromobenzene | HCID 19107866 | — |
Reaction Steps
A solution of 1-bromohexane (9.33 g) in acetone (20 ml) is added dropwise to a stirred mixture of 4-bromo-3-fluorophenol (9.00 g) and potassium carbonate (13.5 g) in acetone 75 ml) at room temperature. The stirred mixture is heated under reflux for 21 h (i.e. until glc analysis revealed a complete reaction). The product is extracted into ether twice, and the combined ether extracts are washed with water, 10% sodium hydroxide, water and dried (MgSO4). The solvent is removed under vacuo and the residue is distilled (bp 100°-105° C. at 0.1 mm Hg) to yield a colourless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05273680 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-858bbcdcf57d47bd8a71f61f772d3446 |
| Source note | uspto-grants-1993_12 |