HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 1H-Indole, 1-acetyl-3-(4-methoxybenzoyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ketone, indol-3-yl p-methoxyphenyl (6CI,8CI) | HCID 211017 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1H-Indole, 1-acetyl-3-(4-methoxybenzoyl)- | HCID 3062673 | — |
Reaction Steps
1 g of compound 1 was added to the mixture of 50 ml each of acetic anhydride and pyridine, and then the solution was stirred overnight at room temperature. The reaction mixture was evaporated to dryness under reduced pressure. The resulting crude crystals were recrystallized from chloroform to obtain 3-(p-methoxybenzoyl)-N-acetylindole (compound 5) in the form of white crystals. (Yield: 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04708961 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-cb4f39a777544bb4bd0ed26adce89ece |
| Source note | uspto-grants-1987_11 |