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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55416생성일: 2026년 10월 25일

Vinyl chloroformate → (3aRS,7SR,7aRS)-7-methyl-7-phenyl-2-vinyloxycarbonyl-4-perhydroisoindolone

https://huagongshe.com/reaction/55416

반응식

참여 물질

역할이름HCID투입량
반응물Vinyl chloroformateHCID 78808—
반응물(3aRS,7SR,7aRS)-2-benzyl-7-methyl-7-phenyl-4-perhydroisoindoloneHCID 67714154—
용매1,2-DichloroethaneHCID 11—
생성물(3aRS,7SR,7aRS)-7-methyl-7-phenyl-2-vinyloxycarbonyl-4-perhydroisoindoloneHCID 67714243—

반응 단계

To a solution of 9 g of (3aRS,7SR,7aRS)-2-benzyl-7-methyl-7-phenyl-4-perhydroisoindolone in 100 cm3 of 1,2-dichloroethane are added, at room temperature, 2.84 cm3 of vinyl chloroformate, followed by heating for 2 hours at reflux. The solution is concentrated to dryness under reduced pressure (2.7 kPa) and the residue is purified by chromatography on a Column of silica gel (particle size 0.04-0.06 mm, diameter 4 cm, height 23 cm), eluting under a pressure of 0.5 bar of nitrogen with a mixture of cyclohexane and ethyl acetate (90/10 by volume) and collecting 100 cm3 fractions. Fractions 17 to 34 are combined and concentrated to dryness under reduced pressure (2.7 kPa). 4.27 g of (3aRS,7SR,7aRS)-7-methyl-7-phenyl-2-vinyloxycarbonyl-4-perhydroisoindolone are obtained in the form of a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624950
출처 데이터셋uspto-grants-1997_04
ORD IDord-d20b4a6c9ecd497384027e92240e0851
출처 메모uspto-grants-1997_04