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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 784Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/784

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[2-(1,3-Dioxan-2-yl)ethoxy]benzaldehydeHCID 19693467—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventDiethyl EtherHCID 3283—
Product2-[2-(4-Vinylphenoxy)ethyl]-[1,3]-dioxaneHCID 1969346877.6%

Reaction Steps

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##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723258
Source datasetuspto-grants-1998_03
ORD IDord-7962a8e3cbfa49e3aabf54e37edc9672
Source noteuspto-grants-1998_03