HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-Acetyl-6-bromo-3,3-dimethylindolin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-acetyl-6-bromo-3-methyl-1,3-dihydro-2H-indol-2-one | HCID 10825759 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Acetyl-6-bromo-3,3-dimethylindolin-2-one | HCID 10826719 | — |
Reaction Steps
To 1-acetyl-6-bromo-3-methyl-1,3-dihydro-2H-indol-2-one (9.5 g) were added NaH (1.57 g), methyl iodide (2.45 ml) and THF (70 ml) under ice-cooling, and the mixture was stirred at room temperature for 2 hours. After the reaction was complete, water was added to the reaction solution, and the mixture was extracted with ethyl acetate solution. This ethyl acetate solution was washed with water and an aqueous sodium chloride solution, dried over magnesium sulfate, filtered, and concentrated. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=4/1) to give the title compound (5.2 g) as a colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08389511B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-6aae1b14ef714dce8814ba9c97231da7 |
| Source note | uspto-grants-2013_03 |