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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 371136생성일: 2026년 10월 26일

1,3-Cyclohexadiene → 3a-(3,4-difluorophenyl)-3a,4,7,7a-tetrahydro-2-methyl-4,7-ethano-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/371136

반응식

참여 물질

역할이름HCID투입량
반응물1,3-CyclohexadieneHCID 11605—
반응물3-(3,4-difluorophenyl)-1-methyl-1H-pyrrole-2,5-dioneHCID 13519570—
용매ChloroformHCID 6212—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
생성물3a-(3,4-difluorophenyl)-3a,4,7,7a-tetrahydro-2-methyl-4,7-ethano-1H-isoindole-1,3(2H)-dioneHCID 13519564—

반응 단계

A 5.0 g amount of 3-(3,4-difluorophenyl)-1-methyl-1H-pyrrole-2,5-dione was dissolved in 25 ml of chloroform with warming. The solution was cooled to room temperature and 2.0 g of cyclohexadiene was added. After prolonged standing another 11/2 ml of diene was added with a small amount of butylated hydroxytoluene. The solution was heated at reflux for 24 hours. The reaction mixture was subjected to high pressure liquid chromatography using a silica gel column and 20% ethyl acetate in hexane as eluent giving 4.9 g of 3a-(3,4-difluorophenyl)-3a,4,7,7a-tetrahydro-2-methyl-4,7-ethano-1H-isoindole-1,3(2H)-dione as a white solid, mp 125°-127° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04529736
출처 데이터셋uspto-grants-1985_07
ORD IDord-28eebc703d3b42c4b0d28ce79db8d281
출처 메모uspto-grants-1985_07