正十一胺

正十一胺是一种有机化合物,化学式为C11H25N。它可由正十一腈[1]或1-硝基十一烷[2]的还原反应制得。十二烷酰胺和次氯酸钠反应,也能得到正十一胺。[3]它和氟硼酸反应,生成氟硼酸正十一铵(C11H23NH3BF4[4],和盐酸发生类似反应,生成相应的盐酸盐[5]。它可以发生甲基化反应,生成N,N-二甲基正十一胺。[6]

正十一胺
别名 1-十一胺
1-氨基十一烷
十一烷胺
识别
CAS号 7307-55-3  checkY
SMILES
 
  • CCCCCCCCCCCN
性质
化学式 C11H25N
摩尔质量 171.32 g·mol−1
熔点 17 °C(290 K)
沸点 242 °C(515 K)
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

参考文献

  1. Rosa Adam, Elisabetta Alberico, Wolfgang Baumann, Hans-Joachim Drexler, Ralf Jackstell, Henrik Junge, Matthias Beller. . Chemistry - A European Journal. 2016-03-24, 22 (14): 4991–5002 [2021-01-14]. doi:10.1002/chem.201504709 (英语).
  2. Petros L. Gkizis, Manolis Stratakis, Ioannis N. Lykakis. . Catalysis Communications. 2013-06, 36: 48–51 [2021-01-14]. doi:10.1016/j.catcom.2013.02.024. (原始内容存档于2020-10-01) (英语).
  3. Dhananjay S. Rane, Man M. Sharma. . Journal of Chemical Technology AND Biotechnology. 1994-03, 59 (3): 271–277 [2021-01-14]. ISSN 0268-2575. doi:10.1002/jctb.280590310 (英语).
  4. Giorgio Olivo, Giulio Farinelli, Alessia Barbieri, Osvaldo Lanzalunga, Stefano Di Stefano, Miquel Costas. . Angewandte Chemie International Edition. 2017-12-18, 56 (51): 16347–16351 [2021-01-14]. doi:10.1002/anie.201709280 (英语).
  5. Limanov, V. E.; Ivanov, S. B.; Sukiasyan, A. N.; Skvortsova, E. K. Synthesis and antimicrobial activity of compounds obtained from higher alkylamines. Khimiko-Farmatsevticheskii Zhurnal, 1981. 15 (6): 35-39. ISSN: 0023-1134.
  6. Md.A.R. Jamil, Abeda S. Touchy, Md. Nurnobi Rashed, Kah Wei Ting, S.M.A. Hakim Siddiki, Takashi Toyao, Zen Maeno, Ken-ichi Shimizu. . Journal of Catalysis. 2019-03, 371: 47–56 [2021-01-14]. doi:10.1016/j.jcat.2019.01.027 (英语).
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