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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53564생성일: 2026년 10월 23일

2-Pyridinecarboxaldehyde → E-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propene

https://huagongshe.com/ko/reaction/53564

반응식

참여 물질

역할이름HCID투입량
반응물2-PyridinecarboxaldehydeHCID 14273—
반응물2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromideHCID 2724168—
반응물3-(1,3-Dioxan-2-yl)-1-(2-pyridyl)-1-propeneHCID 53923275—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물E-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propeneHCID 19694130—
생성물Z-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propeneHCID 70113689—

반응 조건

온도0 °C

반응 단계

(E and Z)-3-(1,3-Dioxan-2-yl)-1-(2-pyridyl)-1-propene (148 and 149). To a suspension of 4.6 g (10.2 mmol) of [2-(1,3-dioxan-2-yl)ethyl]triphenylphosphonium bromide (Aldrich Chemical Co.) in 50 mL of THF at 0° C. was added 6.4 mL (10.2 mmol) of n-butyl lithium (1.6M in hexanes) and the resulting red solution was allowed to stir at 0° C. for 0.5 h. To this solution was added 880 μL (9.3 mmol) of 2-pyridinecarboxaldehyde (Aldrich Chemical Co.). The reaction mixture was allowed to stir at room temperature for 1 h and was then poured into water and partitioned with ether. The combined either extracts were dried over MgSO4 and concentrated. Flash chromatography (elution with 3:1 hexane:ethyl acetate) gave 0.43 g of E-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1 -propene (148) and 1.12 g of Z-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propene (149). 1H NMRs consistent with structures.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620971
출처 데이터셋uspto-grants-1997_04
ORD IDord-321cdd4893b44debad54cad867cbe1e8
출처 메모uspto-grants-1997_04