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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 129587생성일: 2026년 10월 24일

Toluene → 2-[2-(3-Methoxyphenoxy)phenyl]-1,3-dioxolane

https://huagongshe.com/ko/reaction/129587

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물3-MethoxyphenolHCID 9007—
반응물Potassium HydroxideHCID 14797—
반응물2-(2-Bromophenyl)-1,3-dioxolaneHCID 553534—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-[2-(3-Methoxyphenoxy)phenyl]-1,3-dioxolaneHCID 1512571587.1%

반응 조건

온도80 °C

반응 단계

Potassium hydroxide pellets (35.2 g; 0.63 mol) were dissolved in water (50 ml) and 3-methoxyphenol (78 g; 0.63 mol) was added together with toluene (250 ml). The mixture was heated to and maintained at reflux temperature until water ceased to distil over (a total of 65 ml of water was collected). The mixture was cooled to 80° C. and 2-(2-bromophenyl)-1,3,-dioxolane (120 g; 0.524 mol), DMF (200 ml) and cuprous chloride (0.2 g) were added. The mixture was slowly heated to 150°-155° C. and toluene was distilled off. The mixture was maintained at 150°-155° C. for 6 hours then cooled to 25° C. and water (500 ml) was added. The mixture was filtered and the residue was washed with ether (200 ml ). The filtrate was extracted with ether (3×150 ml). The combined ether extracts were washed with 2N sodium hydroxide solution (2×150 ml), water (4×150 ml) and saturated brine (1×200 ml). After drying and filtration the ether solution on evaporation gave 2-[2-(3-methoxyphenoxy)phenyl]-1,3-dioxolane (124.1 g, 87.1% yield) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05468857
출처 데이터셋uspto-grants-1995_11
ORD IDord-1897a7715ce44e0da56d6ff5a8424849
출처 메모uspto-grants-1995_11