HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 6-bromo-2,3-dihydro-1H-indol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1H-Indole-2,3-dione, 6-bromo- | HCID 95716 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 6-bromo-2,3-dihydro-1H-indol-2-one | HCID 2773289 | 64.7% |
Reaction Conditions
| Temperature | 125 °C |
|---|
Reaction Steps
To 6-bromo-1H-indole-2,3-dione (15 g) was added hydrazine (66 ml), and the mixture was stirred at 125° C. for 2 hours. After the reaction was complete, to the mixture was added 6N aqueous HCl solution (60 ml), and the mixture was stirred at 60° C. for 2 hours. After the reaction was complete, the mixture was neutralized with 3N aqueous NaOH solution, and the mixture was extracted with ethyl acetate. This ethyl acetate solution was washed with water and an aqueous sodium chloride solution, dried over magnesium sulfate, filtered, and concentrated to give the title compound (9.1 g) as a red crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08389511B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-d8ee3cc2176045a38d5a45775c7937af |
| Source note | uspto-grants-2013_03 |