Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359479Generated: October 29, 2026

Potassium Iodide → HCID 20065115, compound

https://huagongshe.com/reaction/359479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloro-N,N-dimethylhexan-1-amineHCID 12947031—
ReactantHCID 15135622HCID 15135622—
SolventDimethylformamideHCID 6228—
ProductHCID 20065115HCID 20065115—

Reaction Steps

To 50 ml of dimethylformamide are added 5 g of 2-(4-hydroxyphenoxy)-3-(2-thenoyl)pyridine, 3.5 g of potassium carbonate and 0.5 g of potassium iodide, and the mixture is stirred at room temperature for 30 minutes. Thereto is added 4.1 g of 6-dimethylaminohexyl chloride. The mixture is stirred at 50° C. for 7 hours. Then, the mixture is poured into ice-water, followed by addition of ethyl acetate thereto. The ethyl acetate layer is extracted with hydrochloric acid and the extract is rendered alkaline with potassium carbonate. The isolated oily substance is extracted with ethyl acetate. The extract is washed with water and dried over anhydrous magnesium sulfate. Thereafter, 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-(6-dimethylaminohexyloxy)phenoxy]-3-(2-thenoyl)pyridine fumarate, m.p. 98°-101° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001137
Source datasetuspto-grants-1991_03
ORD IDord-3d1bf7a46be94701880eea4359e25db0
Source noteuspto-grants-1991_03