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HRID 371136作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-CyclohexadieneHCID 11605—
反応物3-(3,4-difluorophenyl)-1-methyl-1H-pyrrole-2,5-dioneHCID 13519570—
溶媒ChloroformHCID 6212—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物3a-(3,4-difluorophenyl)-3a,4,7,7a-tetrahydro-2-methyl-4,7-ethano-1H-isoindole-1,3(2H)-dioneHCID 13519564—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04529736
出典データセットuspto-grants-1985_07
ORD IDord-28eebc703d3b42c4b0d28ce79db8d281
出典メモuspto-grants-1985_07