HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 1-benzenesulfonyl-3-bromo-7-fluoro-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7-Fluoro-1-(phenylsulfonyl)-1H-indole | HCID 11687705 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-benzenesulfonyl-3-bromo-7-fluoro-1H-indole | HCID 59603529 | 95% |
Reaction Steps
To a solution of 1-benzenesulfonyl-7-fluoro-1H-indole (1.00 g, 3.63 mmol) in CCl4 (20 mL) was added a solution of saturated sodium bicarbonate (40 mL) and bromine (0.19 mL, 3.81 mmol) at room temperature. After stirring at room temperature for 16 hours, the reaction was diluted with DCM and water. The organic extract was washed with saturated sodium bicarbonate, 10% aqueous sodium thiosulfate, dried over sodium sulfate, filtered, and concentrated. The product was obtained as an off-white solid (1.22 g, 95%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158625B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-3c5862e76e3f4feb971f97f09d7bf6a5 |
| Source note | uspto-grants-2012_04 |