HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Fluoro-5-methoxybenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | 4-Fluoro-3-methylanisole | HCID 137546 | — |
| Catalyst | Cobalt(II) acetate tetrahydrate | HCID 61372 | — |
| Product | 2-Fluoro-5-methoxybenzoic acid | HCID 2774543 | — |
Reaction Steps
The title compound was prepared according to a method reported by Hay and Blanchard [Canad. J. Chem. 43, 1306 (1965)]. In a three-necked round-bottom flask (1000 mL), equipped with a magnetic stirrer, thermometer, reflux condensor and a gas distribution tube, cobalt(II)acetate tetrahydrate (12.6 g; 51 mmol) was dissolved in glacial acetic acid (404 mL) by stirring. Commercial 4-fluoro-3-methylanisole (35.4, 252 mmol) and 33% HBr in acetic acid (10.1 mL; 51 mmol) were added and then the mixture was heated on an oil-bath to 90°-95° C. All the time a stream of oxygen was passed through the solution at a rate of about 660 mL/min. After 3 hours the reaction mixture was cooled to room temperature and then rotary evaporated to dryness.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05650524 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-5562ccd8fa8e4c149bae787ca5f67172 |
| Source note | uspto-grants-1997_07 |