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) was dissolved in THF (45 mL) and Et3N (3.4 mL, 24.4 mmol) at 0° C. Acetyl chloride (1.5 mL, 21 mmol) was added dropwise. The mixture was stirred at room temperature for 30 minutes. The mixture was partitioned between EtOAc and aqueous HCl. The organic layer was 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 | US08013006B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-3971a915551b4b56a3e6d6cfd651cbcd |
| Source note | uspto-grants-2011_09 |