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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 985575생성일: 2026년 10월 25일

Methanol → 1,4-Dimethoxy-2,5-dimethylbenzene

https://huagongshe.com/reaction/985575

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Dimethyl SulfateHCID 6497—
반응물2,5-Dimethyl-4-benzoquinoneHCID 8718—
반응물Sodium DithioniteHCID 24489—
반응물Sodium MethoxideHCID 10942334—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Ether tetrahydrofuranHCID 21868444—
생성물1,4-Dimethoxy-2,5-dimethylbenzeneHCID 297380—

반응 단계

To a solution of 2,5-dimethyl-1,4-benzoquinone (68.1 g, 0.5 mol) in diethylether:THF (1:1, 800 ml) was added a solution of 80% sodium hydrosulfite (218 g, 1.0 mol) in water (800 ml) and the mixture was stirred for 30 minutes. The organic layer was separated, washed with saturated brine (800 ml), and then dried over anhydrous sodium sulfate. The organic layer was purified by silica gel chromatography with a small amount of silica gel and eluted with THF. The solvent was removed under reduced pressure to obtain 68.9 g as a yellow solid. The crystals were dissolved in ethanol (700 ml). To the solution were added dimethyl sulfate (189 ml, 2.0 mol) and 80% sodium hydrosulfite (21.8 g, 0.1 mol), and then added dropwise a 28% solution of sodium methoxide in methanol (482 ml, 2.5 mol) under reflux. After completion of the addition, the mixture was further stirred under reflux for 3 hours and then the solvent was removed under reduced pressure. The residue was poured into ice-cold water (2000 ml) and extracted with ethyl acetate. The organic layer was separated, washed with saturated brine and dried over magnesium sulfate, and then the solvent was removed under reduced pressure. The residue was purified by silica gel chromatography with a small amount of silica gel and eluted with ethyl acetate:hexane (1:4), and the solvent was removed under reduced pressure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06872718B1
출처 데이터셋uspto-grants-2005_03
ORD IDord-4af2c869e9704421ad62796971427f11
출처 메모uspto-grants-2005_03