HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359481Generated: October 28, 2026
Potassium Iodide → HCID 86744666, compound
https://huagongshe.com/reaction/359481
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-N,N-dimethyl-1-propanamine | HCID 66960 | — |
| Reactant | HCID 15135622 | HCID 15135622 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86744666 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05001137 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-2828b7378b6042d1bc5998c87abaea69 |
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| Source note | uspto-grants-1991_03 |
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