N-苯基哌啶
| N-苯基哌啶 | |
|---|---|
| 別名 | 1-苯基哌啶 |
| 識別 | |
| CAS號 | 4096-20-2 
|
| SMILES |
|
| 性質 | |
| 化學式 | C11H15N |
| 摩爾質量 | 161.24 g·mol−1 |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
N-苯基哌啶是一種有機化合物，化學式為C11H15N。它可由哌啶和溴苯在叔丁醇鉀和鈀催化劑存在下反應製得，[1]它也可以苯胺和1,5-二溴戊烷為原料，在碳酸鉀、碘化鈉存在下於乙腈中回流反應得到。[2]它可以被間氯過氧苯甲酸氧化為N-苯基哌啶-N-氧化物。[3]
參考文獻
[編輯]- ^ Mohammad Al-Amin. Development of Second Generation Gold-Supported Palladium Material with Low-Leaching and Recyclable Characteristics in Aromatic Amination. J. Org. Chem. 2013, 78, 15, 7575–7581. doi:10.1021/jo4011415.
- ^ Xiaona Rong; et al. Iodine-Mediated Coupling of Cyclic Amines with Sulfonyl Hydrazides: an Efficient Synthesis of Vinyl Sulfone Derivatives. European Journal of Organic Chemistry, 2021. 2021 (4): 701-708. doi:10.1002/ejoc.202001510.
- ^ Ju Hyeon An; et al. Highly Chemoselective Deoxygenation of N-Heterocyclic N-Oxides Using Hantzsch Esters as Mild Reducing Agents. J. Org. Chem. 2021, 86, 3, 2876–2894. doi:10.1021/acs.joc.0c02805.