HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-(Pyridin-2-yl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methane | HCID 297 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Bromo-5-chloro-2[(methylsulfonyl)acetyl]-3-(2-pyridyl)indole | HCID 13034586 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(Pyridin-2-yl)-1H-indole | HCID 14338096 | — |
Reaction Steps
To 6-bromo-5-chloro-2[(methylsulfonyl)acetyl]-3-(2-pyridyl)indole (2.2 g) in 75 ml of ethanol add 0.175 g of sodium borohydride. After a solution is obtained (about 10 minutes) stir the mixture of another 30 minutes, then slowly add 2 ml of acetic acid. Treat with charcoal, filter and add 100 ml of water to the filtrate to obtain 6-bromo-5-chloro-2[1-hydroxy-2-methylsulfonyl)ethyl]-3-(2-pyridyl)indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04342769 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-1deef84b26d6447797ae878fcc23f1b5 |
| Source note | uspto-grants-1982_08 |