化工进展 ›› 2016, Vol. 35 ›› Issue (07): 2109-2113.DOI: 10.16085/j.issn.1000-6613.2016.07.024

• 工业催化 • 上一篇    下一篇

杯芳冠醚的合成及其催化合成对氟硝基苯

李成龙, 徐珍, 吕早生, 严若康, 刘秋鸽, 吴洋   

  1. 武汉科技大学化学工程与技术学院, 湖北省煤转化与新型碳材料重点实验室, 湖北 武汉 430081
  • 收稿日期:2015-10-12 修回日期:2015-12-01 出版日期:2016-07-05 发布日期:2016-07-05
  • 通讯作者: 徐珍,讲师,研究方向为精细有机化学的合成研究。E-mail:xuzhen@wust.edu.cn。
  • 作者简介:李成龙(1991-),男,本科。
  • 基金资助:
    2014年湖北省大学生创新创业训练计划项目(201410488033)。

Synthesis of calixcrown ethers and its catalytic activity in synthesis of 4-fluoronitrobenzene

LI Chenglong, XU Zhen, LÜ Zaosheng, YAN Ruokang, LIU Qiuge, WU Yang   

  1. Chemical Engineering Academy of Wuhan University of Science and Technology, Hubei Coal Conversion and New Carbon Materials Key Laboratory, Wuhan 430081, Hubei, China
  • Received:2015-10-12 Revised:2015-12-01 Online:2016-07-05 Published:2016-07-05

摘要: 卤素交换氟化反应是合成含氟芳香化合物的重要方法之一,相转移催化剂对卤素交换氟化反应来说几乎是不可或缺的。本文以对叔丁基杯[4]芳烃和四甘醇二对甲苯磺酸酯为原料,在K2CO3存在下,合成了对叔丁基杯[4]-冠-5,将对叔丁基杯[4]-冠-5作为相转移催化剂应用于对氯硝基苯的氟化反应中,以检测其作为相转移催化剂在氟化反应中的催化活性,同时考察了反应时间、反应温度、不同相转移催化剂对卤素交换氟化反应的影响。结果表明对叔丁基杯[4]-冠-5对氟化反应具有相转移催化能力,研究发现以杯芳冠醚作相转移催化剂,使产品收率得到了明显提高。在对叔丁基杯[4]-冠-5的催化下,反应3h,反应的转化率和收率分别为96.53%、90.8%。

关键词: 有机化合物, 卤素交换氟化, 催化

Abstract: Halogen-exchange fluorination is the main method to synthesize fluorinated aromatics. Phase transfer catalysts (PTCs) are essential for the halogen-exchange fluorination. The p-tert-butylcalix[4]-arene- crown-5 was synthesized from p-tert-butylcalix[4]arene and tetraethylene glycol ditosylate in the presence of K2CO3, and it was used as the phase transfer catalyst in the fluoridation of chlorine nitrobenzene to investigate its performance in the fluorination. The influences of fluorination reaction conditions, such as the reaction time, temperature and different catalysts were investigated. The catalytic activities of p-tert-butylcalix[4]arene- crown-5 were verified. It was found that the yields of the reaction with p-tert-butylcalix[4]arene-crown-5 as PTC were improved. Catalyzed by p-tert-butylcalix[4]arene-crown-5 for 3 h, the reaction had a conversion of 96.53% and the yield of 4-fluoronitrobenzene was 90.8%.

Key words: organic compounds, halogen exchange fluorination, catalysis

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