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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604393Generated: October 30, 2026

Potassium Iodide → HCID 10957911, compound

https://huagongshe.com/reaction/604393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Amino-1-hexanolHCID 19960—
ReactantThionyl ChlorideHCID 24386—
Reactant4-ChloroquinolineHCID 69140—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
SolventTriethylamineHCID 8471—
ProductHCID 10957911HCID 10957911—

Reaction Conditions

Temperature70 °C

Reaction Steps

6-Aminohexanol (15 mmol), 4-chloroquinoline (15 mmol), 5 ml of triethylamine and catalytic amounts of potassium iodide were refluxed in ethanol for 12 hours. The solvent was evaporated and the residue was purified by flash chromatography on silica gel (eluent: methylene chloride/methanol (98/2), ammonia atmosphere). The solvent was removed under reduced pressure. At 0° C. the product (5 mmol) was added to thionyl chloride (10 mmol). The temperature was raised to 70° C. for three hours. Excess thionyl chloride was evaporated. The residue was recrystallized from diethyl ether/ethanol. The product (5 mmol), piperidine (10 mmol), potassium carbonate (15 mmol), and catalytic amounts of potassium iodide were refluxed in acetone for 12 hours. The solvent was evaporated and the residue purified by flash chromatography (eluent: ethyl acetate/methanol/triethylamine (95/5/2)). The solvent was removed under reduced pressure. The residue was crystallized with oxalic acid from diethyl ether/ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910605B2
Source datasetuspto-grants-2011_03
ORD IDord-8ffd15fe8e0a4fedadf0861fd025df4f
Source noteuspto-grants-2011_03