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