HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-indol-4-ol → Indoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-indol-4-ol | HCID 75421 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Indoline | HCID 10328 | — |
Reaction Steps
4-Hydroxyindole was reduced with sodium cyanoborohydride and acetic acid to give 4-hydroxy, dihydroindole. A mixture of ethyl iodide (40 ml), potassium carbonate (1.09 gm, 7.8 mmole) and 4-hydroxy, dihydroindole (1.06 gm, 7.8 mmole) was refluxed for 2 hr. Excess ethyl iodide was evaporated under vacuum, water was added (10 ml) and the product was extracted with dichloromethane. Silica gel chromatography gave N-ethyl4-hydroxy-dihydroindole (0.30 gm, 23% yield) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06713622B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-29d0782979cc489c81f2eac701f8cfcf |
| Source note | uspto-grants-2004_03 |