関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 7,7-Diphenylhexahydro-1H-isoindol-4(2H)-one hydrochloride | HCID 21264543 | — |
| 生成物 | (3As,7as)-7,7-diphenylperhydroisoindol-4-one d-mandelate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05484804 |
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| 出典データセット | uspto-grants-1996_01 |
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| ORD ID | ord-db1548c250864f7dae3da9d3efcb89f5 |
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| 出典メモ | uspto-grants-1996_01 |
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