2-氰基-3-(4-硝基苯基)丙烯酸甲酯
| 2-氰基-3-(4-硝基苯基)丙烯酸甲酯 | |
|---|---|
acrylate.png)
| |
| 別名 | α-氰基對硝基肉桂酸甲酯 |
| 識別 | |
| CAS號 | 62985-31-3  42348-04-9（2E） 14479-59-5（Z）
|
| 性質 | |
| 化學式 | C11H8N2O4 |
| 摩爾質量 | 232.19 g·mol⁻¹ |
| 熔點 | 172—173 °C（445—446 K）[1] 178 °C（451 K）[2] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
2-氰基-3-(4-硝基苯基)丙烯酸甲酯是一種有機化合物，化學式為C11H8N2O4。它可由4-硝基苯甲醛和氰乙酸甲酯在哌啶催化下於甲醇中反應得到。[3]它和氯氣發生加成反應，得到α,β-二氯-α-氰基-4-硝基苯丙酸甲酯。[4]
參考文獻
[編輯]- ^ Lange, J.; Rump, S.; Galecka, E.; Ilczuk, I.; Lechowska-Postek, M.; Rabsztyn, T.; Szymanska, T.; Walczyna, K. Synthesis and properties of new cyclic derivatives of succinic acid with anticonvulsant activity. Pharmazie, 1977. 32 (2): 82-84. ISSN: 0031-7144.
- ^ Saeed Balalaie, Morteza Bararjanian, Shohreh Hekmat, Peyman Salehi. Novel, Efficient, and Green Procedure for the Knoevenagel Condensation Catalyzed by Diammonium Hydrogen Phosphate in Water. Synthetic Communications. 2006-08-01, 36 (17): 2549–2557 [2021-05-17]. ISSN 0039-7911. doi:10.1080/00397910600781471 （英語）.
- ^ Katie M. Herbert, Patrick T. Getty, Neil D. Dolinski, Jerald E. Hertzog, Derek de Jong, James H. Lettow, Joy Romulus, Jonathan W. Onorato, Elizabeth M. Foster, Stuart J. Rowan. Dynamic reaction-induced phase separation in tunable, adaptive covalent networks. Chemical Science. 2020, 11 (19): 5028–5036 [2021-05-17]. ISSN 2041-6520. doi:10.1039/D0SC00605J （英語）.
- ^ Zvi Rappoport, Bianca Avramovitch. Nucleophilic attacks on carbon-carbon double bonds. 28. Complete and partial stereoconversion in the substitution of methyl (E)- and (Z)-.beta.-chloro-.alpha.-cyano-p-nitrocinnamates by nucleophiles. The Journal of Organic Chemistry. 1982-04, 47 (8): 1397–1408 [2021-05-17]. ISSN 0022-3263. doi:10.1021/jo00347a003 （英語）.