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新法合成5-硝基香兰酸

5-nitrovanillic acid:A new synthesis
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摘要 目的:研究了5-硝基香兰酸的合成方法。方法:以4-甲基愈创木酚为原料,先用乙酸酐将酚羟基保护起来,再通过强氧化剂的氧化作用将甲基氧化为羧基,最后水解得香兰酸,再经硝化制得5-硝基香兰酸。结果:得到亮黄色晶体产物,收率为73%。结论:本法操作简易,原料易得,适合工业生产。 Objective :To study the new synthesis of 5--nitrovanillic acid. Method:5--Nitrovanillic acid was synthesized from 4--methyl guaiacol,which reacted with acetic anhydride to protect phenol hydroxyl,and then the methyl was oxidated by strong oxidizer to become the carboxyl group,and finally vanillic acid was obtained through hydrolysising the compound, followed by nitration at last. Result: The bright yellow crystal product was obtained and an overall yield of production was 73 %. Conclusion:This method is very easy,basic materials can be easily obtained, suitable to the industry production.
出处 《黑龙江医药科学》 2008年第6期26-27,共2页 Heilongjiang Medicine and Pharmacy
基金 佳木斯大学科研项目(编号:2006S16)
关键词 5-硝基香兰酸 合成 中间体 5 -- nitrovanillic acid synthesis intermediate
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参考文献4

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  • 4陈毅平.5-硝基香兰酸的合成[J].中国医药工业杂志,2001,32(5):230-231. 被引量:2

二级参考文献3

  • 1Bernauer K,Borgulya J,Bruderer H,et al.Preparation of 3, 5-disubstituted pyrocatechol derivatives as catechol -O-methyltransferase inhibitors[].AU:.1990
  • 2Hynning PA,Remberger M,Neilson AH.Synthesis and gas-liquid chromatographic analysis and gas chromatographic-mass spectrometric identification of nitrovanillins, chloronitrovanillins, nitroguaiacols, and chloronitroguaiacols[].Journal of Chromatography.1989
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