HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-Benzyloxy-1-methylindole-3-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-(phenylmethoxy)-1H-indole-3-carbaldehyde | HCID 81398 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Benzyloxy-1-methylindole-3-carboxaldehyde | HCID 12283854 | — |
Reaction Steps
5g of 5-Benzyloxyindol-3-aldehyde was dissolved in 50 ml of N,N-dimethylformamide, and 0.84 g of 60% sodium hydride was added under ice-cooling. The reaction solution was stirred at room temperature for 30 minutes, 2.5 ml of methyl iodide was added and stirring was continued at room temperature for 16 hours. The reaction solution was cooled with ice, treated with water and ammonium chloride, and extracted with ethyl acetate and tetrahydrofuran. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and evaporated. The residue was treated with diethyl ether and filtered, to give 4.6 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07544835B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-bd079e0cfbdd467fb15f39e2bfe8729b |
| Source note | uspto-grants-2009_06 |