跳转到内容

4-甲氧基亚苄基丙二腈

维基百科,自由的百科全书
4-甲氧基亚苄基丙二腈
识别
CAS号 2826-26-8  checkY
性质
化学式 C11H8N2O
摩尔质量 184.19 g·mol−1
熔点 115 °C(388 K)[1]
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

4-甲氧基亚苄基丙二腈是一种有机化合物,化学式为C11H8N2O,可由4-甲氧基苯甲醛丙二腈Knoevenagel反应制得。[2][3]它和氨硼烷发生加氢反应,得到4-甲氧基苄基丙二腈。[2]它和2-碘丙烷三乙基铝过氧化苯甲酰的存在下于乙醚中反应,可以得到2-[1-(4-甲氧基苯基)-2-甲基丙基]丙二腈。[4]

参考文献

[编辑]
  1. ^ Dry Media Reaction Procedure for Synthesis of α,β-Unsaturated Acids, α-Cyanoacrylonitriles and α-Cyanoacrylates via Knoevenagel Condensation Using NaHSO 4 ·SiO 2 Catalyst. Journal of the Korean Chemical Society. 2007-08-20, 51 (4): 346–351 [2021-05-31]. ISSN 1017-2548. doi:10.5012/jkcs.2007.51.4.346. (原始内容存档于2018-06-02) (英语). 
  2. ^ 2.0 2.1 Jing Li, Martin J. Lear, Yujiro Hayashi. Direct Cyclopropanation of α‐Cyano β‐Aryl Alkanes by Light‐Mediated Single Electron Transfer Between Donor–Acceptor Pairs. Chemistry – A European Journal. 2021-04, 27 (19): 5901–5905 [2021-05-31]. ISSN 0947-6539. doi:10.1002/chem.202100341 (英语). 
  3. ^ Biwei Yan, Linhong Zuo, Xiaowei Chang, Teng Liu, Manying Cui, Yang Liu, Haiyu Sun, Weipeng Chen, Wusheng Guo. Kinetically Controllable Pd-Catalyzed Decarboxylation Enabled [5 + 2] and [3 + 2] Cycloaddition toward Carbocycles Featuring Quaternary Carbons. Organic Letters. 2021-01-15, 23 (2): 351–357 [2021-05-31]. ISSN 1523-7060. doi:10.1021/acs.orglett.0c03856 (英语). 
  4. ^ Jing-Yuan Liu, Yoeng-Jiunn Jang, Wen-Wei Lin, Ju-Tsung Liu, Ching-Fa Yao. Triethylaluminum- or Triethylborane-Induced Free Radical Reaction of Alkyl Iodides and α,β-Unsaturated Compounds. The Journal of Organic Chemistry. 2003-05-01, 68 (10): 4030–4038 [2021-05-31]. ISSN 0022-3263. doi:10.1021/jo020681b (英语).