戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 23712作成日:2026年10月25日

3-Pyridinecarboxaldehyde → 3-(Oxiran-2-yl)pyridine

https://huagongshe.com/reaction/23712

反応式

関与物質

役割名称HCID仕込み量
反応物3-PyridinecarboxaldehydeHCID 10371—
反応物Sodium HydroxideHCID 14798—
反応物Trimethylsulfonium methyl sulfateHCID 2760871—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物3-(Oxiran-2-yl)pyridineHCID 1331956128.6%

反応条件

温度0 °C

反応手順

To a solution of 2.59 g of 3-pyridinecarboxaldehyde and 62 mg of tetra-n-butylammonium bromide in 60 mL CH2Cl2 at room temperature is added a solution of 10.0 g of trimethylsulfonium methylsulfate in 15 mL H2O. The resulting solution is set stirring and cooled to 0° C. Aqueous NaOH (50% w/w; 40 mL) is added in portions while stirring and the mixture subsequently refluxed for 1 h. After cooling to room temperature, the mixture is filtered and the filtrate extracted with CH2Cl2. The combined extracts are dried over MgSO4, filtered, and concentrated to yield a red oil, which is subjected to Kugelrohr distillation under high vacuum at 150° C. to yield 838 mg of the title compound as a clear, light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852731B2
出典データセットuspto-grants-2005_02
ORD IDord-80408188b07545bfbcf381ecf1bc3f7b
出典メモuspto-grants-2005_02