正十一胺
化合物
正十一胺是一種有機化合物,化學式為C11H25N。它可由正十一腈[1]或1-硝基十一烷[2]的還原反應製得。十二烷酰胺和次氯酸鈉反應,也能得到正十一胺。[3]它和氟硼酸反應,生成氟硼酸正十一銨(C11H23NH3BF4)[4],和鹽酸發生類似反應,生成相應的鹽酸鹽[5]。它可以發生甲基化反應,生成N,N-二甲基正十一胺。[6]
正十一胺 | |
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別名 | 1-十一胺 1-氨基十一烷 十一烷胺 |
識別 | |
CAS號 | 7307-55-3 |
SMILES |
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性質 | |
化學式 | C11H25N |
摩爾質量 | 171.32 g·mol−1 |
熔點 | 17 °C(290 K) |
沸點 | 242 °C(515 K) |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
參考文獻
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- ^ Petros L. Gkizis, Manolis Stratakis, Ioannis N. Lykakis. Catalytic activation of hydrazine hydrate by gold nanoparticles: Chemoselective reduction of nitro compounds into amines. Catalysis Communications. 2013-06, 36: 48–51 [2021-01-14]. doi:10.1016/j.catcom.2013.02.024. (原始內容存檔於2020-10-01) (英語).
- ^ Dhananjay S. Rane, Man M. Sharma. New strategies for the Hofmann reaction. Journal of Chemical Technology AND Biotechnology. 1994-03, 59 (3): 271–277 [2021-01-14]. ISSN 0268-2575. doi:10.1002/jctb.280590310 (英語).
- ^ Giorgio Olivo, Giulio Farinelli, Alessia Barbieri, Osvaldo Lanzalunga, Stefano Di Stefano, Miquel Costas. Supramolecular Recognition Allows Remote, Site-Selective C−H Oxidation of Methylenic Sites in Linear Amines. Angewandte Chemie International Edition. 2017-12-18, 56 (51): 16347–16351 [2021-01-14]. doi:10.1002/anie.201709280 (英語).
- ^ 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.
- ^ 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. N-Methylation of amines and nitroarenes with methanol using heterogeneous platinum catalysts. Journal of Catalysis. 2019-03, 371: 47–56 [2021-01-14]. doi:10.1016/j.jcat.2019.01.027 (英語).