関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2-Cyclohexen-1-one, 4,4-dimethyl- | HCID 136839 | — |
| 反応物 | N-Benzyl-1-butoxy-N-[(trimethylsilyl)methyl]methanamine | HCID 11097910 | — |
| 触媒 | Trifluoroacetic acid | HCID 6422 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (3aRS,7aRS)-2-benzyl-7,7-dimethyl-4-perhydroisoindolone | HCID 67714335 | — |
反応手順
To a solution of 5 g of 4,4-dimethylcyclohex-2-enone and 12.4 cm3 of N-butoxymethyl-N-trimethylsilylmethylbenzylamine in 100 cm3 of dichloromethane are added, at a temperature of 10° C., 5 drops of trifluoroacetic acid. The reaction mixture is stirred at this temperature for 3 hours, then potassium carbonate is added and the solution is filtered through a sinter funnel and concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a column of silica gel (particle size 0.04-0.06 mm, diameter 5.2 cm, height 25 cm), eluting under a pressure of 0.5 bar of nitrogen with a mixture of cyclohexane and ethyl acetate (85/15 by volume) and collecting 100 cm3 fractions. Fractions 39 to 63 are combined and concentrated to dryness under reduced pressure (2.7 kPa). 3.64 g of (3aRS,7aRS)-2-benzyl-7,7-dimethyl-4-perhydroisoindolone are obtained in the form of a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05624950 |
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| 出典データセット | uspto-grants-1997_04 |
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| ORD ID | ord-b19dfe6fd32d4b9786df94ca62e8fc2f |
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| 出典メモ | uspto-grants-1997_04 |
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