4-溴苯甲腈
| 4-溴苯甲腈 | |
|---|---|
| |
| 识别 | |
| CAS号 | 623-00-7 
|
| PubChem | 12162 |
| 性质 | |
| 化学式 | C7H4BrN |
| 摩尔质量 | 182.02 g·mol−1 |
| 密度 | 1.85 g·cm−3[1] |
| 熔点 | 114 °C[2] |
| 沸点 | 236 °C[2] |
| 溶解性（水） | 194 μg·mL−1 （pH=7.4 磷酸盐缓冲溶液）[1] |
| log P | 2.1[1] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
4-溴苯甲腈是一种有机化合物，化学式为C7H4BrN。
合成与反应
4-溴苯甲腈可由4-溴苯甲醛和盐酸羟胺在催化下反应得到；[3]或由4-溴甲苯的氨氧化反应制得。[4]
它在三氟甲磺酸的存在下可以三聚，得到2,4,6-三(4-溴苯基)-1,3,5-三嗪：[5]
参考文献
- ^ 1.0 1.1 1.2 Yuki Ichikawa, Michiaki Hiramatsu, Yusuke Mita, Makoto Makishima, Yotaro Matsumoto, Yui Masumoto, Atsuya Muranaka, Masanobu Uchiyama, Yuichi Hashimoto, Minoru Ishikawa. meta -Non-flat substituents: a novel molecular design to improve aqueous solubility in small molecule drug discovery. Organic & Biomolecular Chemistry. 2021, 19 (2): 446–456 [2022-01-13]. ISSN 1477-0520. doi:10.1039/D0OB02083D （英语）.
- ^ 2.0 2.1 "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2021-12-28].
- ^ Tukaram S Choudhare, Devendra S Wagare, Sagar E Shirsath, Prashant D Netankar. H3PO4 catalyzed one-pot synthesis of 1,3-diphenyl-1H-pyrazole-4-carbaldehyde to novel 1,3-diphenyl-1H-pyrazole-4-carbonitrile. Journal of Chemical Sciences. 2021-09, 133 (3) [2021-12-28]. ISSN 0974-3626. doi:10.1007/s12039-021-01939-w （英语）.
- ^ Patent US4124631: Process for the production of aromatic nitriles. Angemeldet am 10. März 1977, veröffentlicht am 7. November 1978, Anmelder: Nippon Kayaku K.K., Erfinder: H. Hayami, H. Shimizu.
- ^ Matthias Bohle et al.: Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 17 Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag, Stuttgart 2004, ISBN 3-13-118671-2, pp. 50.