肉桂基氯
外觀
肉桂基氯 | |
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別名 | 苯丙烯基氯 |
識別 | |
CAS號 | 2687-12-9 ![]() |
性質 | |
化學式 | C9H9Cl |
摩爾質量 | 152.62 g·mol−1 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
肉桂基氯是一種有機化合物,化學式為C9H9Cl。它可由肉桂醇和氯化亞碸[1]或乙酰氯[2]反應製得。它和六甲基二鍺在Pd2(dba)3催化下反應,得到肉桂基三甲基鍺。[3]它和三甲基氰硅烷在銅化合物催化下反應,可以得到4-苯基-3-丁烯腈。[4]
參考文獻
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- ^ Veejendra K Yadav, K Ganesh Babu. Acetyl chloride–ethanol brings about a remarkably efficient conversion of allyl acetates into allyl chlorides. Tetrahedron. 2003-11, 59 (46): 9111–9116 [2023-03-25]. doi:10.1016/j.tet.2003.09.063. (原始內容存檔於2018-06-24) (英語).
- ^ Taichi Nakano, Sigeyuki Nöda, Nao-aki A-ihara, Hirohide Yamashita, Takashi Miyamoto, Toshihiko Migita†, Tatsuki Enokido, Masanori Kosugi. HIGH-YIELD FORMATION OF ALLYLIC GERMANES BY Pd2(dba)3-CATALYZED REACTION OF ALLYLIC HALIDES WITH DIGERMANES. Main Group Metal Chemistry. 2001-01, 24 (2) [2023-03-25]. ISSN 2191-0219. doi:10.1515/MGMC.2001.24.2.67. (原始內容存檔於2023-03-25).
- ^ Daisuke Munemori, Hiroaki Tsuji, Kenta Uchida, Tomoaki Suzuki, Kazuki Isa, Maki Minakawa, Motoi Kawatsura. Copper-Catalyzed Regioselective Allylic Cyanation of Allylic Compounds with Trimethylsilyl Cyanide. Synthesis. 2014-07-09, 46 (20): 2747–2750 [2023-03-25]. ISSN 0039-7881. doi:10.1055/s-0034-1378322. (原始內容存檔於2018-06-02) (英語).