1,4-二(三氟甲基)苯
1,4-二(三氟甲基)苯 | |
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別名 | 對二三氟甲苯 α,α,α,α',α',α'-六氟對二甲苯 |
識別 | |
CAS號 | 433-19-2 ![]() |
SMILES |
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性質 | |
化學式 | C8H4F6 |
摩爾質量 | 214.11 g·mol−1 |
熔點 | 115—117 °C(388—390 K)[1] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
1,4-二(三氟甲基)苯是一種有機化合物,化學式為C8H4F6。它可由4-三氟甲基苯硼酸和三氟甲基亞銅(或其配合物[2])反應製得。[3]三氟乙酸鈉也可作為三氟甲基化試劑與對三氟甲基碘苯反應,得到1,4-二(三氟甲基)苯。[4]它在硫酸-三氟乙酸中回流後加入NBS反應,可以得到1,4-二溴-2,5-二(三氟甲基)苯。[5]它和三溴化硼在四氯化碳中反應,可以得到1,4-二(三溴甲基)苯。[6]
參考文獻
- ^ Yagupol'skii, L. M.; Shein, S. M.; Krasnosel'skaya, M. I.; Solodushenkov, S. N. Preparation of 2-amino-4-trifluoromethylbenzoic acid. Zhurnal Obshchei Khimii, 1965. 35 (7): 1261-1263. ISSN: 0044-460X.
- ^ John Wiley & Sons. E-EROS encyclopedia of reagents for organic synthesis. Hoboken, NJ. [1999]-. ISBN 978-0-470-84289-8. OCLC 48998476.
- ^ Hiroki Serizawa, Kohsuke Aikawa, Koichi Mikami. Direct Synthesis of a Trifluoromethyl Copper Reagent from Trifluoromethyl Ketones: Application to Trifluoromethylation. Chemistry - A European Journal. 2013-12-23, 19 (52): 17692–17697 [2020-10-22]. doi:10.1002/chem.201303828 (英語).
- ^ Carr, G. E.; Chambers, R. D.; Holmes, T. F.; Parker, D. G. ChemInform Abstract: Sodium Perfluoroalkane Carboxylates as Sources of Perfluoroalkyl Groups.. ChemInform. 1988-07-26, 19 (30) [2022-10-01]. doi:10.1002/chin.198830124. (原始內容存檔於2022-10-04) (英語).
- ^ Devic, Thomas; Horcajada, Patricia; Serre, Christian; Salles, Fabrice; Maurin, Guillaume; Moulin, Béatrice; Heurtaux, Daniela; Clet, Guillaume; Vimont, Alexandre; Grenèche, Jean-Marc; Ouay, Benjamin Le. Functionalization in Flexible Porous Solids: Effects on the Pore Opening and the Host−Guest Interactions. Journal of the American Chemical Society. 2010-01-27, 132 (3) [2020-10-22]. ISSN 0002-7863. doi:10.1021/ja9092715. (原始內容存檔於2020-10-08) (英語).
- ^ Chen, Hongbiao; Yin, Jianxiang; Lin, Yuanbin. Mild and efficient conversion of trifluoromethylarenes into tribromomethylarenes using boron tribromide. Chemical Papers. 2009-01-01, 63 (1) [2022-10-01]. ISSN 1336-9075. doi:10.2478/s11696-008-0082-3. (原始內容存檔於2022-10-04).