HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 7-Methoxy-2-methoxy-methylbenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (7-Methoxy-1-benzofuran-2-yl)methanol | HCID 11788606 | — |
| Product | 7-Methoxy-2-methoxy-methylbenzofuran | HCID 70144170 | — |
Reaction Steps
Sodium hydride (3.82 g, 60% in mineral oil) was added to a solution of 7-methoxy-benzofuran-2-ylmethanol (11.21 g) in dry tetrahydrofuran (300 ml) under an atmosphere of dry nitrogen at room temperature. After 10 minutes iodomethane (15.67 ml) was added and the reaction was left to stir overnight. The solvent was removed in vacuo and the residue partitioned between ethyl acetate (100 ml) and water (50 ml). The organic extract was washed with water (50 ml), followed by brine (50 ml), dried over magnesium sulphate, filtered and the solvent removed in vacuo to afford the title compound (13.32 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455561B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-952849ad235d460aa91f7cd0e23da08e |
| Source note | uspto-grants-2002_09 |