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HRID 36832Erstellt: 24. Oktober 2026

Potassium Hydroxide → 4-(Methoxy)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane

https://huagongshe.com/de/reaction/36832

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktBromomethyl methyl etherHCID 83093—
Edukt(1-Methyl-2,6,7-trioxabicyclo[2.2.2]octan-4-yl)methanolHCID 13547990—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
Produkt4-(Methoxy)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octaneHCID 19936244—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

Powdered potassium hydroxide (16.2 g, 0.290 mol) is suspended in 100 mL of dimethyl sulfoxide and the mixture is stirred at 25° C. for 5 min. Then 4-(hydroxymethyl)-1-methyl-2,6,7-trioxabicyclo[2.2.21octane (10.0 g, 0.062 mol) is added followed by bromomethyl methyl ether (9.3 g, 6.1 mL, 0.074 mol). The reaction mixture is stirred for 30 min and then diluted with water (1 L) and extracted with dichloromethane several times. The combined organic layers are washed with saturated sodium chloride (100 mL), dried over anhydrous sodium sulfate and evaporated under reduced pressure to give 4-(methoxy)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octane. This crude material is dissolved in methanol (100 mL) and stirred with pyridinium p-toluenesulfonate (1.6 g, 6.200 mmol) in water (100 mL) for 30 min. The pH of the solution is adjusted to 7 with solid sodium bicarbonate and the solvents are removed under reduced pressure. The resulting solids are triturated with methanol and the methanol solution is evaporated to give 2-(methoxymethoxy)-1,1,1-tris(hydroxymethyl)ethane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05417959
Quelldatensatzuspto-grants-1995_05
ORD IDord-a90a004be91b4ef983749cf4eaaa3e0b
Quellennotizuspto-grants-1995_05