乙酸氯
乙酸氯是一種化合物,化學式為CH3COOCl,可由氯氣的乙酸溶液和乾燥的乙酸汞反應得到。[1]它可用於在有機化合物中引入乙酸酯基(CH3C(=O)O-),[2]如和2-氯-4-甲基苯甲醇反應,得到乙酸(2-氯-4-甲基苯基)甲酯[3];和環己烯反應,得到乙酸-2-氯環己酯[4]。
乙酸氯 | |
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別名 | 次氯酸乙酰酯 |
識別 | |
CAS號 | 758-11-2 |
SMILES |
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性質 | |
化學式 | C2H3ClO2 |
摩爾質量 | 94.5 g·mol−1 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
參考文獻
- ^ De la Mare, P. B. D.; Ketley, A. D.; Vernon, C. A. Chlorine acetate as a reagent for electrophilic chlorine substitution. Research (London), 1953. 6: 12-13S. CAN48: 18058.
- ^ Patrycja Miszczyk, Ilona Turowska-Tyrk, Paweł Kafarski, Ewa Chmielewska. Three-Component Reaction of Benzylamines, Diethyl Phosphite and Triethyl Orthoformate: Dependence of the Reaction Course on the Structural Features of the Substrates and Reaction Conditions. Molecules. 2017-03-11, 22 (3): 450 [2020-04-19]. ISSN 1420-3049. PMC 6155184 . PMID 28287472. doi:10.3390/molecules22030450. (原始內容存檔於2020-02-23) (英語).
- ^ Alemparte-Gallardo, Carlos; Barfoot, Christopher; Barros-Aguirre, David; Cacho-Izquierdo, Monica; Fiandor Roman, Jose Maria; Hennessy, Alan Joseph; Pearson, Neil David; Remuinan-Blanco, Modesto Jesus. Preparation of tricyclic nitrogen containing compounds as antibacterials. 2009. WO 2009141398 A1.
- ^ P. B. D. de la Mare, Charmian J. O'Connor, M. J. Rosser, M. A. Wilson. Cyclic transition states in cis- and trans-addition of chlorine acetate to olefinic substances. Journal of the Chemical Society D: Chemical Communications. 1970, (12): 731 [2020-04-19]. ISSN 0577-6171. doi:10.1039/c29700000731 (英語).