関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | Tellurium | HCID 6327182 | — |
| 反応物 | 3,3-Dibromo-5-(5-bromo-pyridin-3-yl)-pyrrolidin-2-one | HCID 117666948 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-(5-Bromopyridin-3-YL)pyrrolidin-2-one | HCID 117667495 | 74.1% |
反応手順
Sodium borohydride (0.74 g, 19.6 mmol) is suspended in ethanol (17 mL) and tellurium metal powder (1.25 g, 9.78 mmol) is added in portions. The mixture is heated under reflux (external temperature 80° C.) for 15 min and the mixture becomes a light purple color. The mixture is cooled to room temperature. 3,3-Dibromo-5-(5-bromo-pyridin-3-yl)-pyrrolidin-2-one (0.65 g, 1.63 mmol) dissolved in EOH (5 mL) is added slowly. The mixture is stirred at room temperature over the weekend (72 h). The mixture is filtered through diatomaceous earth and washed with MeOH. The filtrate is concentrated. The resulting crude product is purified by normal phase chromatography using 0-6% MeOH in DCM as the gradient to afford 5-(5-bromo-pyridin-3-yl)-pyrrolidin-2-one (291 mg, 74% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09181272B2 |
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| 出典データセット | uspto-grants-2015_11 |
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| ORD ID | ord-499f8385f2b04d57bbd4bd6212d48e5e |
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| 出典メモ | uspto-grants-2015_11 |
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