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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102656Generated: October 31, 2026

Potassium Iodide → 6-Chloro-3,3-bis[(3-chlorophenyl)methyl]-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/2102656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Bromomethyl)-3-chlorobenzeneHCID 69838—
Reactant6-Chloro-1,3-dihydroindol-2-oneHCID 736344—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
Product6-Chloro-3,3-bis[(3-chlorophenyl)methyl]-1,3-dihydro-2H-indol-2-oneHCID 57803075—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 6-chlorooxindole (0.42 g, 2.5 mmol) (Crescent), 3-chlorobenzyl bromide (1.13 g, 5.5 mmol) (Aldrich), potassium iodide (1.04 g, 6.25 mmol) and potassium carbonate (1.04 g, 7.5 mmol) in acetone (10 mL) was heated at 60° C. for 20 hours in a sealed tube. After cooling, mixture was diluted with ethyl acetate (50 mL) and extracted with water (50 mL) and brine (50 mL). Aqueous layers were back washed with ethyl acetate (50 mL). Organic layers were combined, dried (MgSO4), filtered and concentrated. Residue was recrystallized from ethyl acetate-hexanes to give 6-chloro-3,3-bis-(3-chlorobenzyl)-1,3-dihydro-indol-2-one as white needles. (Yield 0.31 g, 29.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576082B2
Source datasetuspto-grants-2009_08
ORD IDord-5e049112aba740ff81c8ced8d1eb3cd7
Source noteuspto-grants-2009_08