HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 3-Allyloxy-4-bromoanisol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-5-methoxyphenol | HCID 13493839 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Allyloxy-4-bromoanisol | HCID 14703422 | 111% |
Reaction Steps
To a solution of 4-bromo-3-hydroxyanisol (14.49, 59.3 mmol), synthesized by known methods, in CH3CN (200 ml), dry potassium carbonate (20 g) and allylbromide (8.0 ml, 92.4 mmol) was added. The reaction mixture was stirred and refluxed for 1 hour and thereafter cooled to room temperature, filtered and evaporated. The residue was dissolved in ether and extracted with water. The organic layer was separated and dried (Na2SO4). Evaporation of the solvent afforded 16.0 g (93%) of 3-allyloxy-4-bromoanisol as an oil. GC/MS (HP-5970A) m/e=244 (40) M+ and M+ -1 at m/e=242 (40), 163 (100), 149 (97), 135 (62).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05306830 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-b51aa913910342a8b842f3b306dd0416 |
| Source note | uspto-grants-1994_04 |