Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 10035244 | HCID 10035244 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Thiosulfate | HCID 24477 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 66788022 | HCID 66788022 | — |
Reaction Steps
Water (25 mL) was added to 4-chloro-1-methyl-1,3-dihydro-indol-2-one (1.25 g, 6.9 mmol) and the resulting mixture was placed at 68° C. In a separate flask potassium bromide (1.64 g, 13.8 mmol) in water (25 mL) was treated with bromine (0.35 mL, 6.9 mmol), the resulting orange solution was added dropwise to the 4-chloro-1-methyl-1,3-dihydro-indol-2-one mixture over ca. 20 minutes. The resulting heterogeneous mixture was permitted to stir at 68° C. for an additional 5 minutes and then cooled to room temperature. The reaction was then diluted with dichloromethane and saturated aqueous sodium bicarbonate. The solution was then further diluted with saturated aqueous sodium thiosulfate. The layers were separated and the aqueous layer was extracted two additional times with dichloromethane. The organic extracts were combined, dried over anhydrous sodium sulfate, filtered and concentrated. The resulting residue was preadsorbed onto silica gel and purified by silica gel flash chromatography (ethyl acetate-heptane 15 to 50%) to provide 5-bromo-4-chloro-1-methyl-1,3-dihydro-indol-2-one; MS: (ES+) m/z 259.9 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778972B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-d2ee6e64bf1840269faa82f0620f711b |
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| Source note | uspto-grants-2014_07 |
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