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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102673Generated: October 30, 2026

Potassium Iodide → HCID 57334375, compound

https://huagongshe.com/reaction/2102673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Bromomethyl)-3-chlorobenzeneHCID 69838—
ReactantHCID 57803077HCID 57803077—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductHCID 57334375HCID 57334375—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 6-chloro-3-(3-methoxy-phenyl)-1,3-dihydro-indol-2-one (0.16 g, 0.6 mmol) (from Example 6b supra), 3-chlorobenzyl bromide (0.15 g, 0.7 mmol)(Aldrich), potassium iodide (0.12 g, 0.71 mmol) and potassium carbonate (0.18 g, 1.3 mmol) in acetone (5 mL) was heated at 60° C. for 4 hours in a capped pressure tube. After cooling, mixture was diluted with ethyl acetate (50 mL) and extracted with water (2×50 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 dichloromethane-hexanes to give rac-6-chloro-3-(3-chloro-benzyl)-3-(3-methoxy-phenyl)-1,3-dihydro-indol-2-one as white needles. (Yield 0.18 g, 75.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576082B2
Source datasetuspto-grants-2009_08
ORD IDord-c1b872fdcce14ee7a788aaf5b8e61f8a
Source noteuspto-grants-2009_08