HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194379Generated: November 1, 2026
Potassium Iodide → 1-(4-chlorobutyl)-4-methylpyridin-2(1H)-one
https://huagongshe.com/reaction/2194379
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-4-chlorobutane | HCID 81364 | — |
| Reactant | HCID 178428601 | HCID 178428601 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-chlorobutyl)-4-methylpyridin-2(1H)-one | HCID 59234645 | 72.8% |
Reaction Steps
A mixture of 2-hydroxy-4-methylpyridine (1.50 g, 13.75 mmol) and potassium carbonate (1.90 g, 13.75 mmol) in 13 ml of methanol were stirred at room temperature for 15 minutes and then 1-bromo-4-chlorobutane (3.54 g, 20.62 mmol) and a spatula tip of potassium iodide were added thereto. The reaction mixture was heated to reflux for 6 hours and then stirred at room temperature for 12 hours. Water was then added to the reaction mixture, and the aqueous mixture was extracted with dichloromethane. Drying of the organic phase and removal of the desiccant by filtration was followed by concentration of the organic phase in vacuo. Flash chromatography of resulting residue on silica gel (eluent: CH2Cl2/CH3OH: 98:2) afforded 2.0 g of 1-(4-chlorobutyl)-4-methylpyridin-2(1H)-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08334289B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-2890c12eea07458a84cc18524000dd1f |
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| Source note | uspto-grants-2012_12 |
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