期刊文献+

4(5)-氰基咪唑的合成与表征

Synthesis and Characterization of 1H-Imidazole-4-Carbonitrile
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摘要 以D-果糖为初始原料,经环合、氧化,再加入盐酸羟胺作为氰基化试剂一步法制得4(5)-氰基咪唑。利用~1H NMR、^(13)C NMR等手段对各步所得产物的结构进行了表征,结果表明产物为4(5)-氰基咪唑。以D-果糖计,3步反应的总收率为33.5%。 ~1H-Imidazole-4-carbonitrile were synthesized with D-fructose as starting materials by cyclization,oxidation and cyanation in a one-spet process by adding hydroxylamine hydrochloride.The structure of the compound was confirmed by ~1H NMR,^(13)C NMR etc.The target product was identified as ~1H-imidazole-4-carbonitrile.The overall yield of fructose was 33.5%in three steps.
出处 《光谱实验室》 CAS CSCD 2012年第1期58-60,共3页 Chinese Journal of Spectroscopy Laboratory
基金 国家自然科学基金资助项目(No.30470388)
关键词 果糖 环合 氧化 氰基化 盐酸羟胺 Fructose Cyclization Oxidation Cyanation Hydroxylamine Hydrochloride
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参考文献3

  • 1Kawakami J I, Kimura K, Yamaoka M. A Convenient Synthesis of 4 (5)-Alkylacyl-lH-Imidazoles from 4 (5)-Imidazolecarboxaldehyde[J]. Synthesis, 2003, (5) : 677-680.
  • 2Matthews D P, Whitten J P, McCarthy J R. A Convenient Procedure for the Preparation of 4 (5)-Cyanoimidazoles[J]. J. Org. Chem. ,1986,51(16):3228-3231.
  • 3Leone-Bay A,Glaser L. An Efficient Method for the Preparation of 4(5)-Cyanoimidazoles[J]. Synth. Commun. , 1987,17(12): 1409--1412.

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