HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 3-(2-Iodoethyl)-5-methoxy-1-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-(5-Methoxy-1-benzofuran-3-yl)ethanol | HCID 14982873 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(2-Iodoethyl)-5-methoxy-1-benzofuran | HCID 23614442 | — |
Reaction Steps
To a stirred solution of 2-(5-methoxy-1-benzofuran-3-yl)ethanol (960 mg, 5 mmol) in anhydrous THF (50 ml), triphenylphosphine (1.572 g, 6 mmol), iodine (1.518 g, 6 mmol) and imidazole (408 mg, 6 mmol) were added at room temperature. The reaction mixture was stirred at room temperature for 4 hrs and quenched with water. It was then extracted with chloroform, washed well with 5% Na2S2O3 and the organic layer dried over anhydrous MgSO4. It was filtered and concentrated. The residue was purified by silica-gel column chromatography by eluting it with 30% ethyl acetate:hexane. The product, 2-(5-methoxy-1-benzofuran-3-yl)ethyl iodide, was obtained as a brown liquid. Yield: 1.1 g (73%); (M+H): 302.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07276603B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-d98cbe5b2ddc462bb5ae73e2d9789a86 |
| Source note | uspto-grants-2007_10 |