참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 7,7-Diphenylhexahydro-1H-isoindol-4(2H)-one hydrochloride | HCID 21264543 | — |
| 생성물 | (3As,7as)-7,7-diphenylperhydroisoindol-4-one d-mandelate | HCID 131719175 | — |
반응 단계
50 cm3 of 4N aqueous sodium hydroxide are added slowly, with stirring, to a suspension of 20 g of (3aRS,7aRS)-7,7-diphenylperhydroisoindol-4-one hydrochloride in 250 cm3 of ethyl acetate; 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 sodium chloride solution, dried over magnesium sulphate and filtered. A solution of 9.3 g of D-(−)-mandelic acid in 50 cm3 of ethyl acetate is added with stirring to the solution thus obtained. 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 brought to reflux with stirring for 15 minutes; the crystals formed are filtered and again crystallized from a mixture of 100 cm3 of acetonitrile and 35 cm3 of distilled water. There are obtained 6.4 g of (3aS,7aS)-7,7-diphenylperhydroisoindol-4-one D-mandelate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06177450B1 |
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| 출처 데이터셋 | uspto-grants-2001_01 |
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| ORD ID | ord-8317e219578d424b857187f3b4d8400a |
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| 출처 메모 | uspto-grants-2001_01 |
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