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HRID 375421作成日:2026年10月25日

Ethyl Acetate → (3As,7as)-7,7-diphenylperhydroisoindol-4-one d-mandelate

https://huagongshe.com/reaction/375421

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium HydroxideHCID 14798—
反応物7,7-Diphenylhexahydro-1H-isoindol-4(2H)-one hydrochlorideHCID 21264543—
生成物(3As,7as)-7,7-diphenylperhydroisoindol-4-one d-mandelateHCID 131719175—

反応手順

50 cm3 of aqueous 4N sodium hydroxide solution are added slowly to a suspension of 20 g of (3aRS,7aRS)-7,7-diphenylperhydroisoindol-4-one hydrochloride in 250 cm3 of ethyl acetate, while stirring; stirring is continued until the starting material has disappeared. The organic solution is washed with 100 cm3 of distilled water and with 100 cm3 of a saturated solution of sodium chloride, dried over magnesium sulphate and filtered. A solution of 9.3 g of D-(-)-mandelic acid in 50 cm3 of ethyl acetate is added to the solution thus obtained, while stirring. The crystals formed are filtered filtered off, washed with 50 cm3 of ethyl acetate (twice) and dried. The crystals are taken up in a solution of 220 cm3 of acetonitrile and 60 cm3 of distilled water and the mixture is refluxed for 15 minutes, while stirring; the crystals formed are filtered off and crystallized again in a mixture of 100 cm3 of acetonitrile and 35 cm3 of distilled water. 6.4 g of (3aS,7aS)-7,7-diphenylperhydroisoindol-4-one D-mandelate are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05484804
出典データセットuspto-grants-1996_01
ORD IDord-db1548c250864f7dae3da9d3efcb89f5
出典メモuspto-grants-1996_01