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HRID 985575作成日:2026年10月26日

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

https://huagongshe.com/reaction/985575

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Dimethyl SulfateHCID 6497—
反応物2,5-Dimethyl-4-benzoquinoneHCID 8718—
反応物Sodium DithioniteHCID 24489—
反応物Sodium MethoxideHCID 10942334—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Ether tetrahydrofuranHCID 21868444—
生成物1,4-Dimethoxy-2,5-dimethylbenzeneHCID 297380—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06872718B1
出典データセットuspto-grants-2005_03
ORD IDord-4af2c869e9704421ad62796971427f11
出典メモuspto-grants-2005_03