戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 53564作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物2-PyridinecarboxaldehydeHCID 14273—
反応物2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromideHCID 2724168—
反応物3-(1,3-Dioxan-2-yl)-1-(2-pyridyl)-1-propeneHCID 53923275—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物E-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propeneHCID 19694130—
生成物Z-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propeneHCID 70113689—

反応条件

温度0 °C

反応手順

(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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05620971
出典データセットuspto-grants-1997_04
ORD IDord-321cdd4893b44debad54cad867cbe1e8
出典メモuspto-grants-1997_04