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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994272Generated: November 1, 2026

Butyl iodide → 1-Butyl-3-hydroxymethyl-2-pyridone

https://huagongshe.com/reaction/1994272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Hydroxymethyl)pyridin-2(1H)-oneHCID 10630482—
SolventDimethylformamideHCID 6228—
Product1-Butyl-3-hydroxymethyl-2-pyridoneHCID 2226647161.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 3-hydroxymethyl-2(11)-pyridone (7-008-01) (0.63 g) in DMF (15 mL), and to the reaction mixture were added potassium carbonate (1.4 g) and 1-iodobutane (1.86 g). After stirring at 70° C. for 2 h, the solvent was removed. To the residue were added a saturated aqueous solution of ammonium chloride and ethyl acetate, and the organic layer was separated, and then the aqueous layer was extracted three times with ethyl acetate. The combined organic layers were washed with water and brine, dried over anhydrous magnesium sulfate, and evaporated under reduced pressure. The obtained crude product was purified by column chromatography (toluene/ethyl acetone=2/1) to give 1-butyl-3-hydroxymethyl-2-pyridone (7-008-02) (0.56 g, 61%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652141B2
Source datasetuspto-grants-2010_01
ORD IDord-8fccb6e95997459d95da9a30f35b0601
Source noteuspto-grants-2010_01