HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 7-Bromo-5-fluoroindolin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-fluoro-1,3-dihydro-2H-indol-2-one | HCID 3731012 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-Bromo-5-fluoroindolin-2-one | HCID 53418888 | 69.6% |
Reaction Steps
A suspension of 5-fluoro-1,3-dihydro-indol-2-one (1.5 g, 10 mmol) in 15 ml of acetonitrile and N-bromosuccinimide (1.8 g, 10 mmol) was stirred at room temperature overnight until the precipitate was formed. The solid was filtered washed with ethanol (5 ml) and dried in vacuo to give 7-bromo-5-fluoro-1,3-dihydro-indol-2-one (1.6 g, 69.6%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08012966B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-37f9eceecd654120add8f8e3f9c5c3b9 |
| Source note | uspto-grants-2011_09 |