関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | Bicyclo(3.2.1)octane-2,4-dione | HCID 144686 | — |
| 反応物 | [Diacetyloxy-(5-chloro-2-methylphenyl)plumbyl] acetate | HCID 178476526 | — |
| 触媒 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 3-(5-Chloro-2-methylphenyl)bicyclo[3.2.1]octane-2,4-dione | HCID 68485517 | 33.3% |
反応手順
To a solution of 5-chloro-2-methylphenyllead triacetate (0.41 g, 0.80 mmol) in chloroform (4 ml) is added bicyclo[3.2.1]octane-2,4-dione (0.10 g, 0.72 mmol) and 4-dimethylaminopyridine (0.46 g, 3.62 mmol), and the reaction mixture is stirred at room temperature for 5 minutes. Next toluene (1 ml) is added, and the mixture is stirred at 80° C. for 1 hour (pre-heated oil bath). The reaction mixture is allowed to cool to room temperature, quenched with 1M hydrochloric acid, and the organic phase separated. The aqueous phase is further washed with dichloromethane (×2), and again the phases are separated. All organics are combined then evaporated under reduced pressure to give a crude oil. Purification by preparative reverse-phase HPLC furnishes 3-(5-chloro-2-methylphenyl)bicyclo[3.2.1]octane-2,4-dione (0.063 g, 33%) as a colourless gum.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08828908B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-52e14d12fcc5455ea0366d1449ee46b8 |
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| 出典メモ | uspto-grants-2014_09 |
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