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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 783생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물4-HydroxybenzaldehydeHCID 126—
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물1,3-Dioxane, 2-(2-bromoethyl)-HCID 520656—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물4-[2-(1,3-Dioxan-2-yl)ethoxy]benzaldehydeHCID 19693467100.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723258
출처 데이터셋uspto-grants-1998_03
ORD IDord-d6f09b988e0848769dd846f380d71108
출처 메모uspto-grants-1998_03