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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858124Generated: October 30, 2026

Iodide Ion → 6-(4-Chloro-benzoyl)-1-methyl-4-(3-trimethylsilanylethynyl-phenyl)-1H-quinolin-2-one

https://huagongshe.com/reaction/1858124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodide IonHCID 30165—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantAluminumHCID 5359268—
Reactant6-(4-Chloro-benzoyl)4-(3-iodo-phenyl)-1-methyl-1H-quinolin-2-oneHCID 15489630—
CatalystCopperHCID 23978—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventDiethylamineHCID 8021—
Product6-(4-Chloro-benzoyl)-1-methyl-4-(3-trimethylsilanylethynyl-phenyl)-1H-quinolin-2-oneHCID 15489631—

Reaction Steps

6-(4-Chloro-benzoyl)4-(3-iodo-phenyl)-1-methyl-1H-quinolin-2-one (9.98 g, 20.0 mMol) was suspended in diethylamine (300 mL). To this solution was added 50 mL of anhydrous N,N-dimethylformamide (DMF), (trimethylsilyl)acetylene (8.5 mL) and bis(triphenylphosphine)-palladium(II) chloride (1.40 g, 2.00 mMol). The flask was covered with aluminum foil and then copper(l) iodide (780 mg, 4.09 mMol) was added causing the reaction mixture to exotherm. After stirring overnight under an atmosphere of dry N2 at ambient temperature, the reaction mixture was concentrated under vacuum and the residue was chromatographed on flash silica gel eluting with a gradient of DCM to MeOH/DCM (2:98) to give 8.55 g of the titled product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150377
Source datasetuspto-grants-2000_11
ORD IDord-1826dddbd62f482f9ef15b150774b06e
Source noteuspto-grants-2000_11