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HRID 36832作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物Bromomethyl methyl etherHCID 83093—
反応物(1-Methyl-2,6,7-trioxabicyclo[2.2.2]octan-4-yl)methanolHCID 13547990—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物4-(Methoxy)-1-methyl-2,6,7-trioxabicyclo[2.2.2]octaneHCID 19936244—

反応条件

温度25 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05417959
出典データセットuspto-grants-1995_05
ORD IDord-a90a004be91b4ef983749cf4eaaa3e0b
出典メモuspto-grants-1995_05