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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708726Generated: November 3, 2026

Sodium Iodide → 6-[6-(4-hydroxypiperidinyl)hexoxy]-3-methoxy-4H-1-benzopyran-4-one

https://huagongshe.com/reaction/1708726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantPiperidin-4-olHCID 79341—
Reactant6-(6-chlorohexoxy)-3-methoxy-4H-1-benzopyran-4-oneHCID 18959698—
SolventMethyl Ethyl KetoneHCID 6569—
Product6-[6-(4-hydroxypiperidinyl)hexoxy]-3-methoxy-4H-1-benzopyran-4-oneHCID 1895972282.8%

Reaction Steps

A mixture of 2 g of 6-(6-chlorohexoxy)-3-methoxy-4H-1-benzopyran-4-one, 1 g of sodium iodide, 0.6 g of potassium carbonate, and 1.4 g of 4-hydroxypiperidine was refluxed in butanone for 96 hours. The solvent was removed and the residue stirred with ethyl acetate and filtered. The solution was washed with water and then dried over sodium sulfate. The solvent was removed to give an oil which was chromatographed over silica gel to give 2 g of 6-[6-(4-hydroxypiperidinyl)hexoxy]-3-methoxy-4H-1-benzopyran-4-one which was converted to the hydrochloride salt by dissolving in ethyl acetate and adding 1 N ethereal HCL: mp 124°-125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359098
Source datasetuspto-grants-1994_10
ORD IDord-a3340a678afa462e8e8b70bcef5e8e5c
Source noteuspto-grants-1994_10