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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276316Generated: November 3, 2026

Hydrogen Bromide → 5-bromo-3,3-dimethyl-2,3-dihydro-1H-indol-2-one

https://huagongshe.com/reaction/1276316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantBromineHCID 24408—
Reactant3,3-Dimethyl-1,3-dihydro-indol-2-oneHCID 313100—
SolventChloroformHCID 6212—
Product5-bromo-3,3-dimethyl-2,3-dihydro-1H-indol-2-oneHCID 12052796—

Reaction Steps

3,3-dimethyl-1,3-dihydro-2H-indol-2-one (1.12 g, 6.95 mmol) was dissolved in chloroform and stirred at room temperature under nitrogen. Bromine (1.12 g) was added and the mixture was heated under reflux until HBr evolution ceased and the bromine colour was discharged from the solution. The solution was washed with sodium metabisulphite solution and sodium hydrogen carbonate solution, dried (MgSO4), filtered and concentrated to dry under reduced pressure to give 5-bromo-3,3-dimethyl-1,3-dihydro-2H-indol-2-one as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166040
Source datasetuspto-grants-2000_12
ORD IDord-43363e9a469342a5add6fe26d9bf116c
Source noteuspto-grants-2000_12