1-(4-氯苯甲酰基)哌啶
| 1-(4-氯苯甲酰基)哌啶 | |
|---|---|
| 识别 | |
| CAS号 | 26163-40-6 
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| SMILES |
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| 性质 | |
| 化学式 | C12H14ClNO |
| 摩尔质量 | 223.7 g·mol−1 |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
1-(4-氯苯甲酰基)哌啶是一种有机氯化合物，化学式为C12H14ClNO。它可由4-三氯乙酰基氯苯或4-氯苯甲酰氯和哌啶反应制得[1][2]。在催化下，它可以被苯基硅烷还原为1-(4-氯苄基)哌啶[3]。
参考文献
[编辑]- ^ Rebelo, Ricardo Andrade; Rezende, Marcos Caroli; Nome, Faruk; Zucco, César. The Use of 2,2,2-Trichloro-1-Arylethanones as Benzoylating Agents. Synthetic Communications. 1987-10, 17 (14): 1741–1748. doi:10.1080/00397918708063993.
- ^ Xie, Weilong; Zhao, Mengdi; Cui, Chunming. Cesium Carbonate-Catalyzed Reduction of Amides with Hydrosilanes. Organometallics. 2013-12-23, 32 (24): 7440–7444. doi:10.1021/om400951n.
- ^ Kelly, Colin M.; McDonald, Robert; Sydora, Orson L.; Stradiotto, Mark; Turculet, Laura. A Manganese Pre‐Catalyst: Mild Reduction of Amides, Ketones, Aldehydes, and Esters. Angewandte Chemie International Edition. 2017-12-11, 56 (50): 15901–15904. doi:10.1002/anie.201709441.