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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 985575Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/985575

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktDimethyl SulfateHCID 6497—
Edukt2,5-Dimethyl-4-benzoquinoneHCID 8718—
EduktSodium DithioniteHCID 24489—
EduktSodium MethoxideHCID 10942334—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelEther tetrahydrofuranHCID 21868444—
Produkt1,4-Dimethoxy-2,5-dimethylbenzeneHCID 297380—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06872718B1
Quelldatensatzuspto-grants-2005_03
ORD IDord-4af2c869e9704421ad62796971427f11
Quellennotizuspto-grants-2005_03