正十一胺

正十一胺
別名	1-十一胺; 1-氨基十一烷; 十一烷胺
識別
CAS號	7307-55-3
SMILES	CCCCCCCCCCCN;
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。

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。十二烷醯胺和次氯酸鈉反應，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]

參考文獻[編輯]

^ Rosa Adam, Elisabetta Alberico, Wolfgang Baumann, Hans-Joachim Drexler, Ralf Jackstell, Henrik Junge, Matthias Beller. NNP-Type Pincer Imidazolylphosphine Ruthenium Complexes: Efficient Base-Free Hydrogenation of Aromatic and Aliphatic Nitriles under Mild Conditions. Chemistry - A European Journal. 2016-03-24, 22 (14): 4991–5002 [2021-01-14]. doi:10.1002/chem.201504709 （英語）.
^ 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）.

[1] Rosa Adam, Elisabetta Alberico, Wolfgang Baumann, Hans-Joachim Drexler, Ralf Jackstell, Henrik Junge, Matthias Beller. NNP-Type Pincer Imidazolylphosphine Ruthenium Complexes: Efficient Base-Free Hydrogenation of Aromatic and Aliphatic Nitriles under Mild Conditions. Chemistry - A European Journal. 2016-03-24, 22 (14): 4991–5002 [2021-01-14]. doi:10.1002/chem.201504709 （英語）.

[2] 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）.

[3] 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）.

[4] 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）.

[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. 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）.

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