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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722686Generated: October 25, 2026

Potassium Iodide → HCID 11759871, compound

https://huagongshe.com/reaction/722686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-BenzenedimethanolHCID 11506—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
ReactantCyclopropyl-4-fluorophenyl ketoneHCID 53737258—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetoneHCID 180—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11759871HCID 11759871—

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution containing 1,4-benzenedimethanol (30 mmol), sodium hydride (25 mmol), catalytic amounts of tetrabutylammonium iodide, and 15-crown-5 (0.5 mmol) in tetrahyrofuran was stirred for 10 minutes. Cyclopropyl-4-fluorophenylketone (20 mmol) was added dropwise, and the solution was refluxed for 24 hours. The solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: methylene chloride/methanol (98/2)). At 0° C. the product (4 mmol) was added to thionyl chloride (8 mmol). The temperature was raised to 70° C. for three hours. Excess thionyl chloride was evaporated and the residue purified by column chromatography on silica gel (eluent: methylene chloride/methanol (95/5)). The product (2 mmol), piperidine (4 mmol), catalytic amounts of potassium iodide, and potassium carbonate (6 mmol) dissolved in acetone were refluxed for 12 hours. The solvent was evaporated. The crude product was washed with water and extracted with ethyl acetate. The organic layer 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 numberUS07138413B1
Source datasetuspto-grants-2006_11
ORD IDord-047a786019534bf185817b78e9825163
Source noteuspto-grants-2006_11