HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(1-Benzofuran-3-yl)ethan-1-one → 1-(Benzofuran-3-yl)-2-bromoethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(1-Benzofuran-3-yl)ethan-1-one | HCID 11286612 | — |
| Reactant | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Benzofuran-3-yl)-2-bromoethanone | HCID 2776580 | 27.4% |
Reaction Steps
A solution of phenyltrimethylammonium tribromide (2.47 g) in tetrahydrofuran (20 ml) was added dropwise at ambient temperature under nitrogen over 5 minutes to a stirred solution of 3-acetylbenzo[b]furan (1 g) in tetrahydrofuran (20 ml), then the mixture was stirred at ambient temperature for a further 1.5 hours, filtered, and the solvent removed in vacuo. The residue was triturated with ether, and the resulting solid was collected by filtration and dried in vacuo at ambient temperature to give 3-(2-bromoacetyl)benzo[b]furan as an off-white solid (0.25 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05869492 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-10b5b665c38b46309fa8f6f6837d9876 |
| Source note | uspto-grants-1999_02 |