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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23712생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/23712

반응식

참여 물질

역할이름HCID투입량
반응물3-PyridinecarboxaldehydeHCID 10371—
반응물Sodium HydroxideHCID 14798—
반응물Trimethylsulfonium methyl sulfateHCID 2760871—
촉매Tetrabutylammonium BromideHCID 74236—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물3-(Oxiran-2-yl)pyridineHCID 1331956128.6%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852731B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-80408188b07545bfbcf381ecf1bc3f7b
출처 메모uspto-grants-2005_02