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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1108006Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1108006

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1-PhenylcyclohexeneHCID 13043—
EduktSodium BicarbonateHCID 516892—
EduktPotassium hydroxy sulfiteHCID 23707502—
KatalysatorWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-Phenyl-7-oxabicyclo[4.1.0]heptaneHCID 10019383%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06063920
Quelldatensatzuspto-grants-2000_05
ORD IDord-94395df33f7f4c38bcdf1e38099dd4be
Quellennotizuspto-grants-2000_05