関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Allyl bromide | HCID 7841 | — |
| 反応物 | Bicyclo(2.2.1)heptan-2-one | HCID 10345 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Tetrahydrofuran hexane | HCID 21883165 | — |
| 生成物 | 3-Allyl-2-norbornanone | HCID 14134638 | — |
反応手順
To 194 ml (388 mmol) of a 2M solution of lithium diisopropyl amide in tetrahydrofuran-hexane, 50 ml of a solution of 38.9 g (353 mmol) of (+)-2-norbornanone in tetrahydrofuran was added dropwise at -40° C., and the mixture was stirred at -20° C. for 30 minutes. Then, 30 ml of a solution of 47.0 g (388 mmol) of allyl bromide in tetrahydrofuran was added dropwise, the mixture was stirred at -20° C. for 30 minutes, the temperature of the mixture was raised to room temperature, and the mixture was stirred for one hour. On ice cooling, the reaction mixture was poured into 300 ml of 2N hydrochloric acid, and the mixture was extracted with toluene (200 ml×4). The extract was washed with successive, saturated sodium bicarbonate solution, water, saturated sodium chloride (each 200 ml), and dried over anhydrous magnesium sulfate. The solution was filtered, and the solvent was distilled off to obtain 77.6 g of crude 3-allyl-2-norbornanone. The crude product was purified by distillation, and 42.5 g (134 mmol) of (+)-exo-3-allyl-2-norbornanone was obtained. Yield: 80%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05266728 |
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| 出典データセット | uspto-grants-1993_11 |
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| ORD ID | ord-cee3979477db4382a9a149016f88b502 |
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| 出典メモ | uspto-grants-1993_11 |
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