乙酰乙酸環己酯
乙酰乙酸環己酯是一種有機化合物,化學式為C10H16O3。它可由乙酰乙酸甲酯或乙酰乙酸乙酯在催化下和環己醇反應製得。[3][4]它和苯乙炔在碳酸銀、乙酸鉀存在下反應,可以得到2-甲基-5-苯基-3-呋喃甲酸環己酯。[5]它和氯化鎂反應,形成配合物。[6]
乙酰乙酸環己酯 | |
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識別 | |
CAS號 | 6947-02-0 |
性質 | |
化學式 | C10H16O3 |
摩爾質量 | 184.23 g·mol−1 |
熔點 | 190—192 °C(463—465 K)[1] |
沸點 | 130—131 °C(403—404 K)(16 torr)[2] |
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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- ^ Alfred R. Bader, Lowell O. Cummings, Henry A. Vogel. Transesterification. I. β-Keto Esters. Journal of the American Chemical Society. 1951-09, 73 (9): 4195–4197 [2021-11-20]. ISSN 0002-7863. doi:10.1021/ja01153a045. (原始內容存檔於2021-11-20) (英語).
- ^ Benjaram M. Reddy, Vangala R. Reddy, Basude Manohar. Mo-ZrO 2 Solid Acid Catalyst For Transesterification of β-Ketoesters. Synthetic Communications. 1999-04, 29 (7): 1235–1239 [2021-11-20]. ISSN 0039-7911. doi:10.1080/00397919908086095 (英語).
- ^ G.C.M. Kondaiah, L. Amarnath Reddy, K. Srihari Babu, V.M. Gurav, K.G. Huge, R. Bandichhor, P. Pratap Reddy, A. Bhattacharya, R. Vijaya Anand. Boric acid: an efficient and environmentally benign catalyst for transesterification of ethyl acetoacetate. Tetrahedron Letters. 2008-01, 49 (1): 106–109 [2021-11-20]. doi:10.1016/j.tetlet.2007.11.008. (原始內容存檔於2020-10-13) (英語).
- ^ Chuan He, Sheng Guo, Jie Ke, Jing Hao, Huan Xu, Hongyi Chen, Aiwen Lei. Silver-Mediated Oxidative C–H/C–H Functionalization: A Strategy To Construct Polysubstituted Furans. Journal of the American Chemical Society. 2012-04-04, 134 (13): 5766–5769 [2021-11-20]. ISSN 0002-7863. doi:10.1021/ja301153k. (原始內容存檔於2021-11-20) (英語).
- ^ L.I. Koval, V.I. Dzyuba, V.V. Bon, O.L. Ilnitska, V.I. Pekhnyo. Synthesis and structure of anhydrous complexes of magnesium(II) with β-ketoesters of higher alcohols. Polyhedron. 2009-09, 28 (13): 2698–2702 [2021-11-20]. doi:10.1016/j.poly.2009.05.034. (原始內容存檔於2022-03-22) (英語).