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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108006Generated: October 26, 2026

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

https://huagongshe.com/reaction/1108006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-PhenylcyclohexeneHCID 13043—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium hydroxy sulfiteHCID 23707502—
CatalystWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1-Phenyl-7-oxabicyclo[4.1.0]heptaneHCID 10019383%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063920
Source datasetuspto-grants-2000_05
ORD IDord-94395df33f7f4c38bcdf1e38099dd4be
Source noteuspto-grants-2000_05