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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398521Generated: October 24, 2026

Methyl iodide → 3-(benzyloxy)-1-methyl-1H-pyridin-2-one

https://huagongshe.com/en/reaction/1398521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178517714HCID 178517714—
SolventDimethyl SulfoxideHCID 679—
Product3-(benzyloxy)-1-methyl-1H-pyridin-2-oneHCID 6818159294.4%

Reaction Steps

To a solution of 3-(benzyloxy)pyridin-2-ol (25 g, 123.00 mmol) and potassium hydroxide (10 g, 178.22 mmol, 1.45 equiv) in dimethylsulfoxide (250 mL) maintained under nitrogen atmosphere was added methyl iodide (27 g, 190.14 mmol) dropwise with stirring. The resulting solution was stirred overnight at room temperature then concentrated under vacuum. The residue was diluted with water (500 mL) then extracted with dichloromethane (2×400 mL). The combined organic layer was washed with water (3×500 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to give the title compound (25 g, 93%) as a light brown oil: 1H NMR (400 MHz, DMSO) delta 7.44-7.32 (m, 5H), 7.29-7.27 (m, 1H), 6.91-6.88 (m, 1H), 6.12-6.09 (m, 1H), 5.02 (s, 2H), 3.44 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901313B2
Source datasetuspto-grants-2014_12
ORD IDord-d333884211c943c4b409461f90bad9cb
Source noteuspto-grants-2014_12