高等学校化学学报 ›› 1984, Vol. 5 ›› Issue (1): 133.
• 研究简报 • 上一篇 下一篇
黄化民1, 李葆2, 战永复2, 沙德有2
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Huang Huamin1, Li Bao2, Zhan Yongfu2, Sha Deyou2
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摘要: 前文已报道,β-二酮类与丙烯腈反应,我们分离出来了一氰乙基化合物,进而异构化为5,6-二取代3,4-二氢化-2(1H)吡啶酮[1]。
Abstract: β-Diketones (butyrylacetone, isobutyrylacetone, isovalerylacetone) were treated with acrylonitrile in the presence of aqueous potassium hydroxide giving monocyanoethylated-β-diketones (Ⅰ)-(Ⅲ), which by heating with HCl were isomerized to the corresponding 3,4-dihydro-2-(1H) pyridones (Ⅳ)-(Ⅵ). (Ⅰ)-(Ⅲ) were hydrolyzed to the ketoacids (Ⅶ)-(Ⅸ). semicarbazone (Ⅹ)-(ⅩⅤ) were prepared from 5-acetyl-6-methyl-3,4dihydyo-2(1H) pyridones; pyrazole(ⅩⅥ)-(ⅩⅨ) were prepared from β-diketoncids. compounds (Ⅰ)-(ⅩⅪ) were reported for the first time.
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黄化民, 李葆, 战永复, 沙德有. 一氰乙基化β-二酮的合成及其异构化(Ⅱ). 高等学校化学学报, 1984, 5(1): 133.
Huang Huamin, Li Bao, Zhan Yongfu, Sha Deyou. MONOCYANOETHYL-β-DIKETONES AND THEIR ISCMERIZATION(Ⅱ). Chem. J. Chinese Universities, 1984, 5(1): 133.
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