HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-[3-Bromo-4-(phenylmethoxy)phenyl]-2-propanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(3-Bromo-4-hydroxyphenyl)propan-2-one | HCID 24721055 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[3-Bromo-4-(phenylmethoxy)phenyl]-2-propanone | HCID 23080563 | — |
Reaction Steps
Potassium carbonate (2.7 g) and benzyl bromide (2.3 ml) were added to a solution of 1-(3-bromo-4-hydroxyphenyl) acetone (4.0 g) in DMF (40 ml) and the mixture was stirred at room temperature for six hours. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate-n-hexane) to obtain 1-[4-(benzyloxy)-3-bromophenyl]acetone (3.65 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07169761B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-03c5e4a9e73a43d2a91aa0627c528459 |
| Source note | uspto-grants-2007_01 |