돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1108006생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1108006

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-PhenylcyclohexeneHCID 13043—
반응물Sodium BicarbonateHCID 516892—
반응물Potassium hydroxy sulfiteHCID 23707502—
촉매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물1-Phenyl-7-oxabicyclo[4.1.0]heptaneHCID 10019383%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06063920
출처 데이터셋uspto-grants-2000_05
ORD IDord-94395df33f7f4c38bcdf1e38099dd4be
출처 메모uspto-grants-2000_05