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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36832Generated: October 26, 2026

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

https://huagongshe.com/reaction/36832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantBromomethyl methyl etherHCID 83093—
Reactant(1-Methyl-2,6,7-trioxabicyclo[2.2.2]octan-4-yl)methanolHCID 13547990—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product4-(Methoxy)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octaneHCID 19936244—

Reaction Conditions

Temperature25 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05417959
Source datasetuspto-grants-1995_05
ORD IDord-a90a004be91b4ef983749cf4eaaa3e0b
Source noteuspto-grants-1995_05