関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 2-Methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-enal | HCID 3017557 | — |
| 反応物 | HCID 178418573 | HCID 178418573 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 2,3-Dimethyl-4-(2,2,3-trimethylcyclopent-3-enyl)butanal | HCID 15431045 | 50.1% |
反応手順
100 ml (0.30 mol) of methylmagnesium bromide solution in diethyl ether was added to 60.0 g (0.32 mol) of cuprous iodide suspended in 350 ml of the same solvent at -10° C., followed by addition of 52.0 g (0.27 mol) of 2-methyl-4-(2,2,3-trimethylcyclopent-3-enyl)but-2-enal dissolved in 300 ml of anhydrous diethyl ether at 0° C. and stirring at the same temperature was continued for 0.5 hours. The reaction mixture was treated with 200 ml of 1.0 N hydrochloric acid, decanted and the organic layer was washed with 2×300 ml of brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (eluent: hexane/MTBE 15:1) to give 28.2 g (50% yield) of 2,3-dimethyl-4-(2,2,3-trimethylcyclopent-3-enyl)butanal.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05929291 |
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| 出典データセット | uspto-grants-1999_07 |
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| ORD ID | ord-9e66560732a1403ebe832736d1a0a33b |
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| 出典メモ | uspto-grants-1999_07 |
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