HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 1-(4-(Benzyloxy)-2-methylphenyl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Hydroxy-1-(2-methylphenyl)ethan-1-one | HCID 21396699 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-(Benzyloxy)-2-methylphenyl)ethan-1-one | HCID 890054 | — |
Reaction Steps
To a solution of Hydroxy-2′-methylacetophenone (5.508 g, 0.037 mol) in DMF (10 mL) is added cesium carbonate (23.8 g, 0.073 mol). The reaction is stirred at room temperature for 10 minutes. Benzyl bromide (4.36 mL, 0.037 mol) is added and after 1 hour at room temperature, the reaction is concentrated under reduced pressure. The residue is dissolved in ethyl acetate and water. The layers are separated and the organic phase is washed with brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound. ES/MS m/e 241.0 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07846960B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-7c0d308bc499469fbbdffb97898ade0a |
| Source note | uspto-grants-2010_12 |