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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 249035생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/249035

반응식

참여 물질

역할이름HCID투입량
반응물Sodium SulfiteHCID 24437—
반응물m-Chloroperbenzoic acidHCID 70297—
반응물Cyclohexen-4-ylmethyl methacrylateHCID 14473552—
반응물PerbenzoateHCID 15871866—
용매DichloromethaneHCID 6344—
생성물(7-Oxabicyclo(4.1.0)heptan-3-yl)methyl 2-methylprop-2-enoateHCID 1464547894.6%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05212252
출처 데이터셋uspto-grants-1993_05
ORD IDord-0c0c4912bbbc430396cee77d9a256554
출처 메모uspto-grants-1993_05