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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376182Generated: October 31, 2026

Potassium Iodide → HCID 11192494, compound

https://huagongshe.com/reaction/1376182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, (3-bromopropoxy)-HCID 68522—
Reactant6-Bromohexanoyl chlorideHCID 89848—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventAcetoneHCID 180—
SolventNitrobenzeneHCID 7416—
SolventEthyl AcetateHCID 8857—
ProductHCID 11192494HCID 11192494—

Reaction Steps

3-Phenoxypropylbromide (10 mmol), piperidine (20 mmol), and catalytic amounts of potassium iodide were refluxed in acetone for 12 hours. The solvent was evaporated. The residue was treated with ethyl acetate. The solvent was removed under reduced pressure, and the product was crystallized with hydrochloric acid from isopropanol/diethyl ether. The product (5 mmol) was added to a solution of 6-bromohexanoylchloride (7.5 mmol) and aluminiumtrichloride (22.5 mmol) in 10 ml of nitrobenzol. The mixture was stirred at room temperature for 3 days. Ethyl acetate was added, and the mixture was extracted with hydrochloric acid (6N). The solution was neutralized with potassium carbonate solution and extracted with methylene chloride. The solvent was removed under reduced pressure. The product (2.5 mmol), piperidine (5 mmol), potassium carbonate (7.5 mmol), and catalytic amounts of potassium iodide were refluxed in acetone for 12 hours. The solvent was evaporated, and the residue was purified by flash chromatography (eluent: methylene chloride/petroleum ether/methanol (96/3/3)). 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 numberUS07169928B2
Source datasetuspto-grants-2007_01
ORD IDord-32ba439cf824436badd62bb5c0f36056
Source noteuspto-grants-2007_01