2-吡啶甲酸苄酯
| 2-吡啶甲酸苄酯 | |
|---|---|
| |
| 別名 | 吡啶-2-甲酸苯甲酯 |
| 識別 | |
| CAS號 | 71653-37-7 
|
| SMILES |
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| 性質 | |
| 化學式 | C13H11NO2 |
| 摩爾質量 | 213.23 g·mol−1 |
| 外觀 | 無色油狀物[1][2] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
2-吡啶甲酸苄酯是一種有機化合物，化學式為C13H11NO2。它可由2-吡啶甲醯氯和苯甲醇在三乙胺存在下反應製得。[3]它和4-氯溴苄反應，可以得到4-氯苄基吡啶鎓-2-甲酸苄酯溴化物。[2]
參考文獻
- ^ Raghunath Reddy Anugu, Sailu Munnuri, and John R. Falck. Picolinate-Directed Arene meta-C–H Amination via FeCl3 Catalysis. J. Am. Chem. Soc. 2020, 142, 11, 5266–5271. doi:10.1021/jacs.9b13753.
- ^ 2.0 2.1 Zhi Yang, Hanlin Chen, Linxi Wan, Xinyi Feng, Lingshuang Ma, Pei Tang, Fen-Er Chen. Sustainable synthesis of long-acting local anesthetics ropivacaine and levobupivacaine under batch and continuous flow via asymmetric hydrogenation. Org. Chem. Front. 2024. 11. 2891-2896. doi:10.1039/D4QO00072B.
- ^ Ju Yuel Baek, Yong-Joo Shin, Heung Bae Jeon, Kwan Soo Kim. Picolinyl group as an efficient alcohol protecting group: cleavage with Zn(OAc)2·2H2O under a neutral condition. Tetrahedron Letters. 2005. 46 (31): 5143-5147. doi:10.1016/j.tetlet.2005.05.125.