戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1398521作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Potassium HydroxideHCID 14797—
反応物HCID 178517714HCID 178517714—
溶媒Dimethyl SulfoxideHCID 679—
生成物3-(benzyloxy)-1-methyl-1H-pyridin-2-oneHCID 6818159294.4%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08901313B2
出典データセットuspto-grants-2014_12
ORD IDord-d333884211c943c4b409461f90bad9cb
出典メモuspto-grants-2014_12