5,6,7,8-四氢异喹啉
外观
5,6,7,8-四氢异喹啉 | |
---|---|
![]() | |
识别 | |
CAS号 | 36556-06-6 ![]() |
性质 | |
化学式 | C9H11N |
摩尔质量 | 133.19 g·mol−1 |
外观 | 无色液体[1] |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
5,6,7,8-四氢异喹啉是一种有机化合物,化学式为C9H11N,它是1,2,3,4-四氢异喹啉的同分异构体。它可由异喹啉和氢气在[BMMIM]NTf2-环辛烷中反应制得。[2]它也可由异喹啉在超酸存在下和环己烷反应得到。[1]它和碘甲烷反应,可以得到N-甲基-5,6,7,8-四氢异喹啉鎓碘化物。[3]
参考文献
[编辑]- ^ 1.0 1.1 Konstantin Yu. Koltunov, G. K. Surya Prakash, Golam Rasul, George A. Olah. Superacidic Activation of Quinoline and Isoquinoline; Their Reactions with Cyclohexane and Benzene 1. The Journal of Organic Chemistry. 2007-09-01, 72 (19): 7394–7397 [2022-12-10]. ISSN 0022-3263. doi:10.1021/jo070875x. (原始内容存档于2022-12-10) (英语).
- ^ Hannelore Konnerth, Martin H. G. Prechtl. Selective hydrogenation of N-heterocyclic compounds using Ru nanocatalysts in ionic liquids. Green Chemistry. 2017, 19 (12): 2762–2767 [2022-12-10]. ISSN 1463-9262. doi:10.1039/C7GC00513J (英语).
- ^ Beata Jędrzejewska, Barbara Michalak. Synthesis and spectroscopic investigation of cationic donor‐(π‐bridge)‐acceptor dye, 4‐[ N ‐(5,6,7,8‐tetrahydroisoquinolinium‐5‐ylidene)methyl]‐ N , N ‐dialkylaniline iodide. Coloration Technology. 2011-10, 127 (5): 288–296 [2022-12-10]. ISSN 1472-3581. doi:10.1111/j.1478-4408.2011.00311.x. (原始内容存档于2022-12-10) (英语).