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N-Alkylation of Aniline by Copper-Chromite Catalyzer by Auto-Transfer Hydrogen Methodology

Mohammad Pouresmaeily Seyed, Shirkavand H Behzad, Shahidzadeh Mansour and Ebrahimi Sobhan


Most alkylations are typically conducted using alcohols, not alkyl halides. Alcohols are less expensive than alkyl halides and their alkylation does not produce salts, the disposal of which can be problematic. Key to the alkylation of alcohols is the use of catalyst that renders the hydroxyl group a good leaving group. The largest scale N-alkylation is the production of the methylamines from ammonia and methanol, resulting in approximately 500,000 tons/year of methylamine, dimethyl-amine, and trimethylamine. The reaction is poorly selective, requiring separation of the three products. Many other industrially significant alkyl amines are produced, again on a large scale, from the alcohols. Epoxides are another class of halide-free N-alkylating agents, useful in the production of ethanolamines, in the last years, leading the N-Alkylation amines reaction by alcohols in the presence of Cu catalyzer to act in low pressure and temperature conditions. Among the used catalyzers can point Cu-Acetate (Cu(OAC)2) and Cu-Oxide (CuO) also Aniline with Benzyl alcohol reaction.


索引于

  • 中国社会科学院
  • 谷歌学术
  • 打开 J 门
  • 中国知网(CNKI)
  • 引用因子
  • 宇宙IF
  • 米亚尔
  • 秘密搜索引擎实验室
  • 欧洲酒吧
  • 巴塞罗那大学
  • ICMJE

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