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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249011Generated: November 3, 2026

Potassium Iodide → HCID 13753877, compound

https://huagongshe.com/reaction/1249011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2',4'-Dihydroxy-3'-propylacetophenoneHCID 2775198—
ReactantHCID 13779396HCID 13779396—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
ProductHCID 13753877HCID 1375387781%

Reaction Steps

A mixture of 9.77 g of 1-(2,4-dihydroxy-3-propylphenyl)ethanone, 10.90 g of 1-(tetrahydro-2-pyranoxy)-6-chloro-2-hexyne [R. B. Moffet, P. H. Seay and W. R. Reid, J. Med. Pharm. Chem., 14, 1075 (1971)]. 10.43 g of anhydrous potassium carbonate and 8.36 g of potassium iodide in 250 ml of anhydrous acetone was stirred at reflux for 18 hours. Anhydrous dimethyl formamide (100 ml) was added and reflux with stirring was continued for 52 hours. The solvent was removed in vacuo, the residue was stirred with hexane and filtered. The filtrate was concentrated in vacuo to an oil which was dissolved in 300 ml of methanol and 200 ml of 3N hydrochloric acid and heated on the steam bath for 45 minutes. As the solvent was being removed in vacuo, crystallization occurred. Water was added and the solid was filtered to give 11.78 g, mp 88°-90°, (81% yield) of 1- [2-hydroxy-4-[(6-hydroxy-4-hexynyl)oxy]-3-propylphenyl]ethanone, the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04628115
Source datasetuspto-grants-1986_12
ORD IDord-5c00f337af3446f790ae1d25f2227bab
Source noteuspto-grants-1986_12