HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489255Generated: October 28, 2026
Butyl iodide → 1-Butyl-5,6-dimethyl-3-methoxy-2-pyridone
https://huagongshe.com/reaction/489255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 22266504 | HCID 22266504 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 1-Butyl-5,6-dimethyl-3-methoxy-2-pyridone | HCID 22266538 | 29.6% |
Reaction Steps
n-Butanol (13 mL) was added to a mixture of 5,6-dimethyl-3-methoxy-2-pyridone (1-004-06) (306 mg) and potassium hydroxide (157 mg). 1-Iodobutane (0.44 mL) was added to the suspension, and the reaction mixture was heated with stirring in an oil bath at 85° C. under nitrogen atmosphere. After 24 h, the reaction mixture was evaporated under reduced pressure, and the residue was dissolved in acetyl acetate and water. The reaction mixture was extracted twice with ethyl acetate, and once with water, dried over magnesium sulfate, and evaporated under reduced pressure. The obtained residue (300 mg) was purified by silica gel column chromatography (Lobar column B, toluene/acetone (3/1)) to give 1-butyl-5,6-dimethyl-3-methoxy-2-pyridone (1-004-07) (124 mg, 29.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06977266B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-a201b319f91643c183f75278ec4ad7c2 |
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| Source note | uspto-grants-2005_12 |
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