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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623523Generated: November 2, 2026

Bromine → HCID 66788022, compound

https://huagongshe.com/reaction/1623523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantPotassium BromideHCID 253877—
ReactantHCID 10035244HCID 10035244—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium ThiosulfateHCID 24477—
SolventSodium BicarbonateHCID 516892—
ProductHCID 66788022HCID 66788022—

Reaction Conditions

Temperature68 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778972B2
Source datasetuspto-grants-2014_07
ORD IDord-d2ee6e64bf1840269faa82f0620f711b
Source noteuspto-grants-2014_07