HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 1-(6-Nitroindolin-1-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Nitroindoline | HCID 29757 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(6-Nitroindolin-1-yl)ethanone | HCID 258566 | 100.7% |
Reaction Steps
6-Nitroindoline (3.0 g, 18.3 mmol) is dissolved in THF (45 mL) and Et3N (3.4 mL, 24.4 mmol) at 0° C. Acetyl chloride (1.5 mL, 21 mmol) is added dropwise. The mixture is stirred at room temperature for 30 minutes. The mixture is partitioned between EtOAc and aqueous HCl. The organic layer is dried and concentrated to yield 1-acetyl-6-nitroindoline (3.8 g, 100%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781478B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-bbf0a277953b4ec3897b702dccdbc346 |
| Source note | uspto-grants-2010_08 |