参与物
| 角色 | 名称 | HCID | 投料 |
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| 反应物 | 4-[2-(1,3-Dioxan-2-yl)ethoxy]benzaldehyde | HCID 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]-dioxane | HCID 19693468 | 77.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US05723258 |
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| 来源数据集 | uspto-grants-1998_03 |
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| ORD ID | ord-7962a8e3cbfa49e3aabf54e37edc9672 |
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| 来源说明 | uspto-grants-1998_03 |
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