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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709921Generated: October 29, 2026

Potassium Iodide → HCID 23036309, compound

https://huagongshe.com/reaction/1709921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(3-Chloropropoxy)-3-methoxyacetophenoneHCID 7314264—
ReactantHCID 15020357HCID 15020357—
Solvent1-ButanolHCID 263—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
ProductHCID 23036309HCID 2303630967.4%

Reaction Steps

A mixture of α,α-bis(4-fluorophenyl)-3-pyrrolidineacetonitrile (5.13 g, 0.0172 mole), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone (4.17 g, 0.0172 mole), and potassium carbonate (5.53 g, 0.04 mole) was heated overnight at reflux in 350 ml of 1-butanol containing potassium iodide (0.2 g). The butanol was removed by rotary evaporation. The residue obtained was dissolved in chloroform and extracted several times with water. The chloroform layer was dried over sodium sulfate, filtered, and solvent removed in vacuo to give a dark brown oil. The oil was subjected to flash chromatography on silica gel using ethyl acetate and 25% methanol-75% ethyl acetate for elution. Fractions of similar purity were combined and solvents removed. A dark brown oil was obtained and dried in vacuo 2 days at 80° C. to give 5.85 g (57.5% yield) of the title compound as a dark brown gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950674
Source datasetuspto-grants-1990_08
ORD IDord-2a9572346ded4efe8454b7784548446a
Source noteuspto-grants-1990_08