1,3二羟基山酮的c -丙烯酰化:合成、表征及抗菌活性

E. Yuanita, Baiq Khaeratul Jannah, M. Ulfa, Sudirman, Baiq Nila Sari Ningsih, N. K. T. Dharmayani
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引用次数: 0

摘要

以丙烯基溴和KOH为原料成功合成了戊烯基1,3-二羟基山酮。利用红外光谱(IR)和核磁共振(1H-NMR)对合成的化合物进行表征,发现在2号碳上发生了单取代的c-戊烯酰化反应,生成1,3-二羟基-2-戊烯基口山酮。合成结果为黄褐色糊状物,收率为43.09%。该戊基化1,3-二羟基山酮对大肠杆菌具有中等抑菌活性,浓度为15%时抑菌带为bb0 ~ 5mm。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
C-prenylation of 1,3 dihydroxyxanthone: synthesis, characterization and antibacterial activity
Prenylated 1,3-dihydroxyxanthone has been successfully synthesized using Prenyl bromide and KOH. Characterization of the synthesized compound using Infra Red (IR) and Nuclear Magnetic Resonance (1H-NMR) showed that monosubstituted c-prenylation was occurred at carbon number 2 to form 1,3-dihydroxy-2-prenylxanthone. The synthesis result was a yellow-brown paste with a yield of 43.09%. This prenylated 1,3-dihydroxyxanthone had moderate antibacterial activity against Escherichia coli with an inhibition zone > 5 mm at a concentration of 15%.
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