HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorophenol → Benzene, 1-(3-buten-1-yloxy)-4-fluoro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Benzene, 1-(3-buten-1-yloxy)-4-fluoro- | HCID 18971814 | 36% |
Reaction Steps
A solution of 4-bromo-1-butene (4.0 g), 4-fluorophenol (3.0 g), potassium carbonate (3.8 g) and acetone (75 ml) was heated at reflux over 16 hours. The mixture was then concentrated in vacuo, dluted with ether, washed with water followed by 1N sodium hydroxide, dried over sodium sulfate, filtered, and concentrated in vacuo. Chromatography on a silica gel column eluting with 25% ethyl acetate-hexane afforded 1.6 g of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05814651 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-8da0142d35ed43beaa759a5b59177616 |
| Source note | uspto-grants-1998_09 |