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HRID 784生成日期:2026年10月23日

4-[2-(1,3-Dioxan-2-yl)ethoxy]benzaldehyde → 2-[2-(4-Vinylphenoxy)ethyl]-[1,3]-dioxane

https://huagongshe.com/zh-CN/reaction/784

反应方程式

参与物

角色名称HCID投料
反应物4-[2-(1,3-Dioxan-2-yl)ethoxy]benzaldehydeHCID 19693467—
反应物叔丁醇钾HCID 23665647—
催化剂甲基三苯基溴化膦HCID 74505—
溶剂乙醚HCID 3283—
产物2-[2-(4-Vinylphenoxy)ethyl]-[1,3]-dioxaneHCID 1969346877.6%

反应步骤

In another 2 liter flask, 57.2 g of methyl triphenylphosphonium bromide was placed. 500 ml of anhydrous ether was poured and then, stirred. To the resulting solution was slowly added 18.0 g of potassium tert-butoxide and reacted at room temperature for 3 hrs. 25.6 g of the above 4-(2-[1,3]-dioxane-2-yl-ethoxy)benzaldehyde was dissolved in 200 ml of anhydrous ether and was slowly added to the reaction mixture and then subjected to reaction at room temperature for 4 hrs. After completion of the reaction, the produced solid by-product was filtered off and washed with distilled water and saturated saline. The organic phase washed was dried over anhydrous magnesium sulfate and the solvent was removed by distillation under reduced pressure. The reaction mixture was purified by Silica gel column chromatography to obtain 19.7 g of 2-[2-(4-vinylphenoxy)ethyl]-[1,3]-dioxane, represented by the following formula: ##STR9##

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US05723258
来源数据集uspto-grants-1998_03
ORD IDord-7962a8e3cbfa49e3aabf54e37edc9672
来源说明uspto-grants-1998_03