HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-(Cyclopropyl-methoxy-methyl)-7-methoxybenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Cyclopropyl-(7-methoxybenzofuran-2-yl)-methanol | HCID 18784867 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Cyclopropyl-methoxy-methyl)-7-methoxybenzofuran | HCID 18784860 | — |
Reaction Steps
To a stirred suspension of sodium hydride (60% dispersion in mineral oil, 0.52 g) in tetrahydrofuran (60 ml) under an atmosphere of nitrogen was added slowly a solution of cyclopropyl-(7-methoxybenzofuran-2-yl)-methanol (1.88 g) in tetrahydrofuran (15 ml). After stirring for 5 minutes, iodomethane (1.6 ml) was added and the mixture concentrated in vacuo. The residue was partitioned between ethyl acetate (100 ml) and water (100 ml), the organic layer washed with water (100 ml), separated, dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by flash chromatography on silica eluting with dichloromethane afforded the title compound as a yellow gum (1.62 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06066657 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-6db5ecc150054891ad615a26161b92a0 |
| Source note | uspto-grants-2000_05 |