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HRID 21372作成日:2026年10月25日

Methyl iodide → 4-(1-Methoxyethyl)pyridine

https://huagongshe.com/reaction/21372

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Sodium hydrideHCID 24758—
反応物alpha-Methyl-4-pyridinemethanolHCID 90919—
反応物HCID 178418361HCID 178418361—
溶媒TetrahydrofuranHCID 8028—
生成物4-(1-Methoxyethyl)pyridineHCID 14442203—

反応手順

A solution of 8.4 g (0.068 mol) of 4-(1-hydroxyethyl)pyridine in 20 ml of absolute tetrahydrofuran is added dropwise to a suspension of 2 g (0.083 mol) of sodium hydride (3.3 g of 60% oil dispersion; washed in toluene) in 80 ml of absolute tetrahydrofuran. After the development of hydrogen has ceased, 23 g (0.16 mol) of methyliodide are added at 18°-20° C. and the mixture is left to react for 2 hours. The reaction mixture is concentrated by evaporation, the residue is combined with 40% aqueous potassium carbonate solution and extracted with ether. The organic phase is separated, dried over sodium sulphate and concentrated by evaporation. After distillation of the crude product at 82°-85° C./20 mbar, 5.2 g (55.6% of theory) of the title compound are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05422353
出典データセットuspto-grants-1995_06
ORD IDord-9d0dbd675f6c4d5c966cbe879b8d52b4
出典メモuspto-grants-1995_06