HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921380Generated: October 31, 2026
Potassium Iodide → 3-ethyl-6-methyl-5-thiophen-2-yl-1H-pyridin-2-one
https://huagongshe.com/reaction/1921380
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | HCID 11673096 | HCID 11673096 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-ethyl-6-methyl-5-thiophen-2-yl-1H-pyridin-2-one | HCID 67492268 | 90% |
Reaction Steps
To a solution of 3-ethyl-2-methoxy-6-methyl-5-(thiophen-2-yl)pyridine (6.15 g, 26.36 mmol) of the above reaction, potassium iodide (8.75 g, 52.71 mmol) and acetonitrile (80 mL) is added chlorotrimethylsilane (6.69 mL, 52.71 mmol) and the resulting cloudy mixture is heated to 80° C. for 2 hr. The reaction is cooled, poured into water and the solids collected by filtration, washed with water, with ethyl acetate and dried giving 3-ethyl-6-methyl-5-(thiophen-2-yl)-1H-pyridin-2-one as a yellow solid (90% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173682B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-42de59cfb65848209e4f91f7849f0b89 |
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| Source note | uspto-grants-2012_05 |
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