関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | Tert-butyl 2-(2-oxobut-3-EN-1-YL)pyrrolidine-1-carboxylate | HCID 21988503 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Octahydroindolizin-7-one | HCID 11240524 | 93% |
反応手順
(±)-1-(t-Butoxycarbonyl)-2-(2-oxo-3-butenyl)pyrrolidine (140 mg (0.59 mmol), prepared as described in 2)) was dissolved in tetrahydrofuran (2 ml). To the solution was added an aqueous solution of 1N hydrochloric acid (1.76 ml, 1.76 mmol), and the resulting mixture was stirred at 70° C. for 4 hours. At the end of this time, to the reaction mixture was added a saturated aqueous solution of sodium hydrogencarbonate and the resulting mixture was extracted with dichloromethane. The organic layer was washed with water, dried over anhydrous magnesium sulfate and the solvent was removed by distillation under reduced pressure, to give the title compound (76 mg) as a light brown oil (yield 93%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07091352B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-bd1629c0454e45928b744802850b9f19 |
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| 出典メモ | uspto-grants-2006_08 |
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