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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249035Generated: October 25, 2026

Sodium Sulfite → (7-Oxabicyclo(4.1.0)heptan-3-yl)methyl 2-methylprop-2-enoate

https://huagongshe.com/reaction/249035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantCyclohexen-4-ylmethyl methacrylateHCID 14473552—
ReactantPerbenzoateHCID 15871866—
SolventDichloromethaneHCID 6344—
Product(7-Oxabicyclo(4.1.0)heptan-3-yl)methyl 2-methylprop-2-enoateHCID 1464547894.6%

Reaction Steps

A 8 liter, 4 necked flask equipped with a thermometer, cooling jacket, stirring means and drip funnel was charged with 200 g of cyclohexen-4-ylmethyl methacrylate produced in Step A and 1200 ml of methylene chloride. The reactants were cooled to a temperature below 10° C. A solution of 263.6 g of m-chloroperbenzoic acid (80% purity, Kishida Chemicals) in 2800 ml of methylene chloride was added thereto dropwise over 3 hours and then allowed to react for additional 3 hours with stirring. After the reaction, an amount of 10% aqueous solution of sodium sulfite was added to the reaction mixture and allowed to react at room temperature for 1 hour to decompose unreacted perbenzoate. After having confirmed the absence of perbenzoate using starch-iodine indicator paper, the reaction mixture was washed with 1000 ml of an aqueous solution containing 81 g of sodium carbonate and then with an amount of saline successively. Thereafter the mixture was dried over magnesium sulfate and evaporated under reduced pressure with addition of 40 mg of p-methoxyquinone as a polymerization inhibitor to remove the solvent. 206 g of crude product of the titled compound was obtained. Yied: 95% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212252
Source datasetuspto-grants-1993_05
ORD IDord-0c0c4912bbbc430396cee77d9a256554
Source noteuspto-grants-1993_05