HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 5-Allyloxy-4-bromo-2-fluoroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Amino-2-bromo-4-fluorophenol | HCID 10965651 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Allyloxy-4-bromo-2-fluoroaniline | HCID 21265598 | 32.9% |
Reaction Steps
5-Amino-2-bromo-4-fluorophenol (30.9 g), allyl bromide (21.8 g) and potassium carbonate (22.77 g) were suspended in acetonitrile (300 ml), and the mixture was stirred at room temperature for 12 hours. After the reaction, the precipitates were filtered, the solvent was distilled off, and this was extracted with ethyl acetate. After washing with water, it was dried over anhydrous magnesium sulfate. Then, ethyl acetate was distilled off and the resulting oily substance was purified by chromatography on silica gel (ethyl acetate:n-hexane=1:3) to obtain the objective 5-allyloxy-4-bromo-2-fluoroaniline (12.14 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06174839B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-b3d8c62272b443e0bc028e62b5887f53 |
| Source note | uspto-grants-2001_01 |