Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359481Generated: October 28, 2026

Potassium Iodide → HCID 86744666, compound

https://huagongshe.com/reaction/359481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-N,N-dimethyl-1-propanamineHCID 66960—
ReactantHCID 15135622HCID 15135622—
SolventDimethylformamideHCID 6228—
ProductHCID 86744666HCID 86744666—

Reaction Steps

To 30 ml of dimethylformamide are added 3 g of 2-(4-hydroxyphenoxy)-3-(2-thenoyl)-pyridine, 1.7 g of potassium carbonate and 0.3 g of potassium iodide. The mixture is stirred at room temperature for 30 minutes. Thereto is added 1.5 g of 3-dimethylaminopropyl chloride, and the mixture is stirred at 50° C. for 4 hours. Thereafter, the reaction mixture is poured into ice-water, whereto ethyl acetate is added. The ethyl acetate is extracted with a dilute hydrochloric acid and the extract is rendered alkaline with potassium carbonate. The isolated oily substance is extracted with ethyl acetate. After the extract is washed with water and dried over anhydrous magnesium sulfate, the solvent is distilled off. The residue is converted into the salt with fumaric acid in ethanol. The salt is recrystallized from ethanol to give 2-[4-(3-dimethylaminopropoxy)phenoxy]-3-(2-thenoyl)pyridine fumarate 1/2 hydrate, m.p. 96°-99° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001137
Source datasetuspto-grants-1991_03
ORD IDord-2828b7378b6042d1bc5998c87abaea69
Source noteuspto-grants-1991_03