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HRID 1108006作成日:2026年10月27日

Water → 1-Phenyl-7-oxabicyclo[4.1.0]heptane

https://huagongshe.com/reaction/1108006

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1-PhenylcyclohexeneHCID 13043—
反応物Sodium BicarbonateHCID 516892—
反応物Potassium hydroxy sulfiteHCID 23707502—
触媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物1-Phenyl-7-oxabicyclo[4.1.0]heptaneHCID 10019383%

反応手順

To a solution of phenyl cyclohexene (79 mg, 0.5 mmol) in a mixture of acetonitrile (4.5 ml) and water (2 drops) were added first finely crushed NaHCO3 (168 mg, 2 mmol) and oxone (307 mg, 0.5 mmol) then the catalyst (0.05 mmol). The resulting yellow suspension was allowed to react at RT, under good stirring. TLC was used to follow the reaction which indicated that the reaction was finished in 2 h. Water (3 ml) was added to the reaction mixture followed by extraction into methylene dichloride. The organic extracts were combined and dried over anhydrous sodium sulphate. Concentration on a rotary evaporator gave a material which was purified on a column using 2% ethyl acetate:petrol mixture as eluent to give the desired compound as a colourless oil. (72 mg, 83% yield, 70% e.e).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06063920
出典データセットuspto-grants-2000_05
ORD IDord-94395df33f7f4c38bcdf1e38099dd4be
出典メモuspto-grants-2000_05