2-溴苯酚合成工艺的优化研究
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O625.33

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Optimization of Synthesis Process of 2-Bromophenol
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    摘要:

    2-溴-4-叔丁基苯酚与甲苯的叔丁基转移反应可以形成重要的有机中间体2-溴苯酚。考察了催化剂及反应条件对叔丁基转移反应的影响,结果表明,三氯化铝及其与叔胺盐酸盐的复合盐对叔丁基转移反应的具有较好的催化活性,27AlNMR的分析表明催化活性中心可能是三氯化铝与水解产生的氯化氢反应形成的氯铝酸。进一步研究表明,氯化氢及溴化氢可提高三氯化铝的催化活性,降低三氯化铝的用量。优化后的工艺条件:在二氯甲烷溶剂中,4-叔丁基苯酚与溴素在0℃反应选择性形成2-溴-4-叔丁基苯酚,加入摩尔分数为30%的AlCl3及600%的甲苯,30℃“一锅法”反应制备2-溴苯酚,2-溴-4-叔丁基苯酚反应的转化率及选择性可达96.5%、99.6%。

    Abstract:

    An important organic intermediate 2-bromophenol can be prepared by the tert butyl transfer reaction of toluene with 2-bromo-4-tert-butyl phenol. The effect of catalyst and the reaction condition on the tert butyl transfer reaction of 2-bromo-4-tert-butyl phenol were investigated. The results show that aluminum tri-chloride and its complex salt with tertiary amine and hydrogen chloride are active in the reaction. The analysis of 27Al NMR shows that the real catalytic species may be chloroaluminate, which formed by the reaction of aluminum trichloride with hydrogen chloride from the hydrolysis of aluminum trichloride. Further, the hydrogen chloride and hydrogen bromide are proved to be the aluminum trichloride activator, and the dosage of aluminum trichloride can be reduced. The optimized process condition is as followed : 4-tert butyl phenol reacted with bromine at 0℃in dichloromethane selectively forming 2-bromo-4-tert butyl phenol, then,2-bromophenol can be prepared through “one pot reaction” by adding aluminum tri-chloride and toluene in molar percentage of 30 and 600 at 30℃. The conversion and selectivity of 2-bromo-4-tert butyl phenol are of 96.5% and 99.6%, respectively.

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温声平,宋沙沙,李云庆,王家喜.2-溴苯酚合成工艺的优化研究[J].精细化工,2016,33(9):

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  • 收稿日期:2016-02-18
  • 最后修改日期:2016-05-23
  • 录用日期:2016-05-27
  • 在线发布日期: 2016-08-17
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