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5-溴-3-仲丁基-6-甲基脲嘧啶的合成及表征

任会学12,杨延钊2,林吉茂2,齐银山3,张业清3   

  1. 1. 山东建筑大学市政环境工程学院, 山东 济南 250010;2. 山东大学化学与化工学院, 山东 济南 250001;3. 淄博华联矿业有限公司, 山东 淄博 256100
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2006-10-24 发布日期:2006-10-24
  • 通讯作者: 任会学

Synthesis and characterization of 5-bromo-3-sec-butyl-6-methyluracil

REN Hui-xue12,YANG Yan-zhao2,LIN Ji-mao2,QI Yin-shan3,ZHANG Ye-qing3   

  1. 1. School of Municipal and Environmental Engineering, Shandong Jianzhu Univ.;2. School of Chemistry and Chemical Engineering, Shandong Univ.;3. Zibo Hualian Mining Industry Co Ltd, Zibo 256100
  • Received:1900-01-01 Revised:1900-01-01 Online:2006-10-24 Published:2006-10-24
  • Contact: REN Hui-xue

摘要: 研究了5-溴-3-仲丁基-6-甲基脲嘧啶(除草定)的新合成方法. 以2-溴丁烷和尿素作为起始原料,经缩合、环化、溴代三步反应得到除草定,总收率为61%. 用1HNMR,13CNMR,IR对产物结构进行了表征.

关键词: 除草定, 缩合, 溴代 , 环化

Abstract: A new synthetic method of 5-bromo-3-sec-butyl-6-methyluracil(Bromacil) was described. Bromacil was synthesized using 2-bromobutane and urea as the starting materials in three steps including condensation, cyclization and bromination with total yield of 61%. The structure of Bromacil was characterized by

Key words: bromination , cyclization, condensation, Bromacil

中图分类号: 

  • TQ463.4
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