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HRID 783作成日:2026年10月23日

4-Hydroxybenzaldehyde → 4-[2-(1,3-Dioxan-2-yl)ethoxy]benzaldehyde

https://huagongshe.com/ja/reaction/783

反応式

関与物質

役割名称HCID仕込み量
反応物4-HydroxybenzaldehydeHCID 126—
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物1,3-Dioxane, 2-(2-bromoethyl)-HCID 520656—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物4-[2-(1,3-Dioxan-2-yl)ethoxy]benzaldehydeHCID 19693467100.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723258
出典データセットuspto-grants-1998_03
ORD IDord-d6f09b988e0848769dd846f380d71108
出典メモuspto-grants-1998_03