HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 1-Acetoxy-3-fluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 3-Fluorophenol | HCID 9743 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Acetoxy-3-fluorobenzene | HCID 136542 | — |
Reaction Steps
A solution of 3-fluorophenol (100 g, 0.890 mol) in methylene chloride is cooled to 0° C. to 5° C., treated with pyridine (75.0 mL, 0.930 mol), stirred for several minutes, treated dropwise with acetyl chloride (66.0 mL, 0.930 mol) while maintaining the reaction mixture temperature below 17° C., stirred at ice-bath temperature for two hours, warmed to room temperature, and poured into an ice-water mixture. The organic phase is separated, washed with brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain the title product as a yellow oil which is identified by 1H NMR spectral analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06140270 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-e96d5f65761b43dd830b043a36ffa666 |
| Source note | uspto-grants-2000_10 |