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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492470Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 15280201, compound

https://huagongshe.com/reaction/1492470

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 10760318HCID 10760318—
ReactantSodium BisulfiteHCID 23665763—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 15280201HCID 1528020193.2%

Reaction Steps

m-Chloroperbenzoic acid (777 mg, 4.5 mmoles) was added to a solution of (4S,5S)-4,5-bis(benzoyloxymethyl)-1-cyclohexene (1.05 g, 3.0 mmoles) in methylene chloride (6 ml) under cooling with ice. After stirring the mixture at room temperature for 2 hours, a saturated aqueous solution of sodium hydrogen sulfite was added to the reaction mixture and the excessive peracid was decomposed, after which a saturated aqueous solution of sodium hydrogen carbonate was added and the whole mixture was subjected to extraction with ethyl ether. The ether extract solution was washed with water and then with saturated aqueous solution of sodium hydrogen carbonate, and dried on anhydrous sodium sulfate. After distilling off the solvent therefrom under reduced pressure, the residue was purified by silica gel column chromatography (ethyl acetate:n-hexane=1:3, v/v) to obtain (3S,4S)-3,4-bis(benzoyloxymethyl)-7-oxabicyclo[4.1.0]heptane (1.025 g, Yield 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374625
Source datasetuspto-grants-1994_12
ORD IDord-e2705e36c2b64bd8b4e56b3f93b05f71
Source noteuspto-grants-1994_12