HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Acetylbenzofuran → 1-(1-Benzofuran-2-Yl)-2-Bromoethan-1-One
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Acetylbenzofuran | HCID 15435 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(1-Benzofuran-2-Yl)-2-Bromoethan-1-One | HCID 2735451 | — |
Reaction Steps
Benzofuran-2-yl methyl ketone (20 g) is dissolved in 100 ml of methylene chloride and 3.2 ml of bromine in methylene chloride is added at 5°-10° C. Then the reaction mixture is stirred at +15° C. for 2 hours. Then it is washed with water, with diluted sodium bicarbonate solution and again with water. The organic phase is dried and evaporated to dryness to give crude 1-(benzofuran-2-yl)-2-bromoethanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04689339 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-831b47ccaa75402fb592e9fa15e798c2 |
| Source note | uspto-grants-1987_08 |