二(4-乙醯基苯基)甲烷
化合物
二(4-乙醯基苯基)甲烷是一種酮類有機物,化學式為C17H16O2。它可由二苯基甲烷和乙醯氯在三氯化鋁催化下於二氯甲烷(或二硫化碳[2])反應製得[3]。它在硝酸-硫酸混酸中於3 °C反應,可以得到二(2-硝基-4-乙醯基苯基)甲烷[4]。它可以被次溴酸鈉氧化為二(4-羧基苯基)甲烷[1]。
二(4-乙醯基苯基)甲烷 | |
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別名 | 雙(4-乙醯基苯基)甲烷 |
識別 | |
CAS號 | 790-82-9 ![]() |
性質 | |
化學式 | C17H16O2 |
摩爾質量 | 252.31 g·mol−1 |
外觀 | 白色[1]或淺黃色固體[2] |
熔點 | 93—94 °C(366—367 K)[3] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
參考文獻
- ^ 1.0 1.1 Jeong, Woomin; Khazi, Mohammed Iqbal; Lee, Dong Geol; Kim, Jong-Man. Intrinsically Porous Dual-Responsive Polydiacetylenes Based on Tetrahedral Diacetylenes. Macromolecules. 2018-12-26, 51 (24): 10312–10322. doi:10.1021/acs.macromol.8b02294.
- ^ 2.0 2.1 Truccolo, Giada; Tessari, Zeno; Tessarolo, Jacopo; Quici, Silvio; Armelao, Lidia; Rancan, Marzio. A Cu( ii ) metallocycle for the reversible self-assembly of coordination-driven polyrotaxane-like architectures. Dalton Transactions. 2018, 47 (35): 12079–12084. doi:10.1039/C8DT02693A.
- ^ 3.0 3.1 Zaitsev, B. A.; Shvabskaya, I. D. Divinyl aromatic compounds and Di(methacrylates) prepared by acid-catalyzed transformations of bis[4-(1-hydroxyethyl)phenyl]alkanes. Russian Journal of Applied Chemistry. 2011-10, 84 (10): 1783–1794. doi:10.1134/S1070427211100181.
- ^ Tashiro, Masashi; Yamato, Takehiko; Fukata, Gouki; Fukuda, Yasuhisa. Friedel-Crafts chemistry. 6. Substituent effects on the ipso nitration and the novel nitration of some diphenylmethanes. The Journal of Organic Chemistry. 1981-05, 46 (11): 2376–2379. doi:10.1021/jo00324a032.