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 | Pyridine, hydrobromide (1:1) | HCID 87810 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(1-Benzofuran-2-Yl)-2-Bromoethan-1-One | HCID 2735451 | 120.5% |
Reaction Steps
A polymer of perbromide of pyridine hydrobromide (8.75 g; 17.5 mmol; 1.4 equivalent) is added to a solution of (benzofuran-2-yl)methylketone (2 g; 12.5 mmol) in methanol (40 ml). The resulting mixture is stirred at ambient temperature for 7 hours and the reaction is stopped by filtration. The methanol is eliminated under reduced pressure and an additional addition of diethyl ether allows crystallization of the expected product (3.6 g; yield=60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06727269B1 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-8b062b5ecece4b5c84180c77d59ef961 |
| Source note | uspto-grants-2004_04 |