烯丙胺鹽酸鹽
烯丙胺鹽酸鹽 | |
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識別 | |
CAS號 | 10017-11-5 |
性質 | |
化學式 | C3H8ClN |
摩爾質量 | 93.56 g·mol−1 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
烯丙胺鹽酸鹽是烯丙胺和氯化氫形成的鹽,化學式為C3H8NCl。它可用於聚烯丙胺或聚烯丙胺鹽酸鹽的合成。[1]
製備及反應
烯丙胺鹽酸鹽可由烯丙胺和鹽酸在5 °C反應得到,在60 °C可整去大部分溶劑,然後在−80 °C凍干,得到固體。[2]N-Boc-烯丙胺和氯化氫反應,也能得到烯丙胺鹽酸鹽。[3]N,N-二(三甲基矽基)烯丙胺和鹽酸反應,也能得到該產物。[4]
它在含次磷酸的氫碘酸中煮沸反應,可以得到2-碘丙胺氫碘酸鹽。這一反應在常溫下不會發生。[5]它和氰酸鉀在水中加熱反應,可以得到烯丙基脲。[6]它和硫脲在苯甲醚中於180 °C反應,可以得到烯丙基異硫氰酸酯。[7]
參考文獻
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- ^ Rik H. Verschueren, Philippe Gilles, Seger Van Mileghem, Wim M. De Borggraeve. Solvent-free N -Boc deprotection by ex situ generation of hydrogen chloride gas. Organic & Biomolecular Chemistry. 2021, 19 (26): 5782–5787 [2022-05-02]. ISSN 1477-0520. doi:10.1039/D1OB00728A (英語).
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- ^ Ya Gao, Jinshan Xie, Ruotian Tang, Kaiyin Yang, Yahan Zhang, Lixia Chen, Hua Li. Identification of a pyrimidinetrione derivative as the potent DprE1 inhibitor by structure-based virtual ligand screening. Bioorganic Chemistry. 2019-04, 85: 168–178 [2022-05-02]. doi:10.1016/j.bioorg.2018.12.018 (英語).
- ^ Shinohata, Masaaki; Kosugi, Yuji; Miyake, Nobuhisa. Method for preparation of isothiocyanates and storing the intermediates thiocarbamates. 2014 WO 2014136690 A1.