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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Vinyl chloroformate | HCID 78808 | — |
| 반응물 | (3aRS,7SR,7aRS)-2-benzyl-7-methyl-7-phenyl-4-perhydroisoindolone | HCID 67714154 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | (3aRS,7SR,7aRS)-7-methyl-7-phenyl-2-vinyloxycarbonyl-4-perhydroisoindolone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05624950 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-d20b4a6c9ecd497384027e92240e0851 |
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| 출처 메모 | uspto-grants-1997_04 |
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