HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Fluorophenol → 2-[(3-fluorophenoxy)methyl]oxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Fluorophenol | HCID 9743 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Epibromohydrin | HCID 18430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-[(3-fluorophenoxy)methyl]oxirane | HCID 9989610 | 44.3% |
Reaction Steps
A solution of 3-fluorophenol (1.8 g, 16.1 mmol) in acetone (100 mL) was treated with potassium carbonate (6.65 g, 48.2 mmol) and refluxed under nitrogen for 15 minutes. Epibromohydrin (4.4 g, 32.1 mmol) was then added by syringe, and the mixture was refluxed 3 hours. The mixture was cooled and filtered, and the filtrate evaporated to dryness. The residue was partitioned between ether/water, and the layers separated. The ether layer was washed with saturated NaCl, dried over sodium sulfate and evaporated. The resulting oil was distilled under vacuum to give 1.2 g of 3-fluorophenyl glycidyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06022894 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-262dccfb3bcf471da57dda92679ba839 |
| Source note | uspto-grants-2000_02 |