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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416546Generated: October 30, 2026

Butyl iodide → 1-Butyl-5,6-dimethyl-3-methoxy-2-pyridone

https://huagongshe.com/reaction/416546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 22266504HCID 22266504—
Solvent1-ButanolHCID 263—
Product1-Butyl-5,6-dimethyl-3-methoxy-2-pyridoneHCID 2226653829.6%

Reaction Conditions

Temperature85 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088924B2
Source datasetuspto-grants-2012_01
ORD IDord-f391c593008c49f19914eda53218d2a8
Source noteuspto-grants-2012_01