HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-Acetyl-6-bromo-5-methoxyindoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(6-Bromo-5-hydroxy-2,3-dihydro-1H-indol-1-yl)ethan-1-one | HCID 21948380 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Acetyl-6-bromo-5-methoxyindoline | HCID 21948375 | 88.1% |
Reaction Steps
A stirred solution of 1-acetyl-6-bromoindolin-5-ol (Tetrahedron 1973, 29(8), 1115; 40 g, 0.15 mole) in DMF (500 ml) was treated with K2CO3 (61 g, 0.45 mole) and iodomethane (11.7 ml, 0.19 mole) and maintained at room temperature for 20 h, then concentrated under vacuum to 200 ml. The residue was treated with water (200 ml) and the precipitate filtered off, dried and recrystallised from EtOAc to afford the title compound as a white solid (35.7 g, 85%). MH+ 270/272.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07109201B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-5f997226f28c48008664d4de881b219d |
| Source note | uspto-grants-2006_09 |