HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-fluoro-6-iodo-1-methyl-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-fluoro-6-iodo-1H-indole | HCID 22612772 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-fluoro-6-iodo-1-methyl-1H-indole | HCID 68524290 | 96.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 6-iodo-5-fluoro-1H-indole (0.495 g, 1.890 mmol) in dry DMF (7.0 mL) was added sodium hydride (55% suspension in oil) (0.124 g, 2.840 mmol) at 0° C. The mixture was stirred at 0° C. for 30 min, and then iodomethane (0.15 mL, 2.47 mmol) was added. The mixture was stirred for 1 hour at room temperature, and then quenched with ice and extracted with EtOAc (50 mL). The organic layer was washed with water, brine, dried over MgSO4, filtered, and concentrated. The residue was purified by column chromatography (EtOAc-hexane, 1:9) to afford 5-fluoro-6-iodo-1-methyl-1H-indole as a colorless solid (0.50 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08207216B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-a508b61691fa4a808cabed1c880ca87c |
| Source note | uspto-grants-2012_06 |