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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102665Generated: October 30, 2026

Potassium Iodide → HCID 57803042, compound

https://huagongshe.com/reaction/2102665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 57803085HCID 57803085—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductHCID 57803042HCID 57803042—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of rac-6-chloro-3-(3-chloro-phenyl)-1,3-dihydro-indol-2-one (0.17 g, 0.6 mmol) (from Example 5b supra), benzyl bromide (0.12 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 5 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 purified by flash chromatography (Biotage 40S, dichloromethane, then 5% ethyl acetate in dichloromethane as solvent) to give two products. Lower Rf sample was recrystallized from dichloromethane-hexanes to give rac-3-benzyl-6-chloro-3-(3-chloro-phenyl)-1,3-dihydro-indol-2-one as white needles. (Yield 0.17 g, 76.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576082B2
Source datasetuspto-grants-2009_08
ORD IDord-6ee7ed38041a4c1da29c0a4c029a665e
Source noteuspto-grants-2009_08