3-氟-4-甲基苯甲醛
外观
(重定向自C8H7FO)
| 3-氟-4-甲基苯甲醛 | |
|---|---|
| 识别 | |
| CAS号 | 177756-62-6 |
| PubChem | 2774574 |
| SMILES |
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| 性质 | |
| 化学式 | C8H7FO |
| 摩尔质量 | 138.14 g·mol−1 |
| 外观 | 亮黄色液体[1] |
| 若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 | |
3-氟-4-甲基苯甲醛是一种有机氟化合物,化学式为C8H7FO。它可由4-甲基苯甲醛在乙腈中经10%氟气于0 °C氟化得到,[1]或以3-氟-4-甲基苯甲酸为原料,经多步反应制得。[2]它和乙氧羰基亚甲基三苯基磷在二氯甲烷中反应,可以得到(E)-3-(3-氟-4-甲基苯基)丙烯酸乙酯。[3]
参考文献
[编辑]- ^ 1.0 1.1 Chambers R D, Sandford G, Trmcic J, Okazoe T. Elemental Fluorine. Part 21.1 Direct Fluorination of Benzaldehyde Derivatives. Organic Process Research and Development, 2008. 12 (2): 339-344. doi:10.1021/op700194r.
- ^ Khanna I K, Weier R M, Yu Y, et al. 1, 2-Diarylimidazoles as potent, cyclooxygenase-2 selective, and orally active antiinflammatory agents. Journal of medicinal chemistry, 1997, 40 (11): 1634-1647. doi:10.1021/jm9700225. "Step 1. To a solution of 3-fluoro-4-methylbenzoic acid ... give 11.41 g (86%) of the benzaldehyde as a yellow oil"
- ^ West T H, Walden D M, Taylor J E, et al. Catalytic enantioselective [2, 3]-rearrangements of allylic ammonium ylides: a mechanistic and computational study. Journal of the American Chemical Society, 2017, 139(12): 4366-4375. doi:10.1021/jacs.6b11851. p S57 "Ethyl (E)-3-(3-fluoro-4-methylphenyl)acrylate SI-30"