返回
化工社化工社化学信息打印报告 · 仅供科研参考
HRID 783生成日期:2026年10月23日

对羟基苯甲醛 → 4-[2-(1,3-Dioxan-2-yl)ethoxy]benzaldehyde

https://huagongshe.com/zh-CN/reaction/783

反应方程式

参与物

角色名称HCID投料
反应物对羟基苯甲醛HCID 126—
反应物碘化钾HCID 4875—
反应物碳酸钾HCID 11430—
反应物2-(2-溴乙基)-1,3-二氧杂环己烷HCID 520656—
溶剂乙腈HCID 6342—
溶剂乙酸乙酯HCID 8857—
产物4-[2-(1,3-Dioxan-2-yl)ethoxy]benzaldehydeHCID 19693467100.2%

反应步骤

In a 500 ml flask, 120 ml of acetonitrile, 13.8 g of 4-hydroxybenzaldehyde, 21.1 g of 2-(2-bromoethyl)-1,3-dioxane, 1.8 g of potassium iodide, and 35.8 g of potassium carbonate were placed and then, reacted at 80° C. for 5 hrs. Thereafter, 200 ml of ethyl acetate was added to the reaction mixture and washed once with a saturated aqueous potassium carbonate solution, distilled water, and saturated saline. The washed organic phase was dried over anhydrous magnesium sulfate and removed solvent, to give 25.6 g of 4-(2-[1,3]-dioxane-2-yl-ethoxy)benzaldehyde.

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-d6f09b988e0848769dd846f380d71108
来源说明uspto-grants-1998_03