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羟基磷灰石负载锰催化溴苯的Suzuki反应

Suzuki Reactions of Aryl Bromides Catalyzed by Hydroxyapatite-Supported Manganese

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【作者】 乔江彬朱雯芳卓广澜周浩姜玄珍

【Author】 QIAO Jiangbin1,ZHU Wenfang1,ZHUO Guanglan1*,ZHOU Hao2,JIANG Xuanzhen2(1 Department of Chemistry,Zhejiang Sci-Tech University,Hangzhou 310018,Zhejiang,China;2 Department of Chemistry,Zhejiang University,Hangzhou 310014,Zhejiang,China)

【机构】 浙江理工大学化学系浙江大学化学系浙江大学化学系 浙江杭州310018浙江杭州310018浙江杭州310014

【摘要】 以羟基磷灰石(HAP)负载Mn作为催化剂(MnHAP)催化溴苯与苯硼酸的Suzuki交叉偶联反应.以氟离子交换羟基磷灰石的羟基(MnFAP)后,催化剂的活性显著提高,在优化的反应条件下能得到约70%的产率.进一步考察了溶剂和不同取代基的影响.结果表明,MnFAP作用下溶剂极性对反应有很大影响,当溶剂DMF/H2O比例为1/3时产率最高.对于不同取代基取代的溴代芳烃或苯硼酸,可以得到中等产率(18%~46%)的偶联产物.

【Abstract】 Suzuki cross-coupling reactions between aryl bromides and phenylboronic acids were studied over a hydroxyapatite-supported Mn catalyst(MnHAP) for the first time.An increased yield was obtained over the fluoride ion-exchanged hydroxyapatitesupported Mn catalyst(MnFAP).Under optimized conditions,the yield was about 70%.The effect of solvent compositions and different substituents were studied over the MnFAP catalyst.The DMF-H2O mixture with a DMF/H2O volume ratio of 1/3 was the best solvent.Moderate yields(18%-46%) were obtained for all tested aryl bromides and phenylboronic acids substituted by different groups.

【基金】 国家自然科学基金(20476092)
  • 【文献出处】 催化学报 ,Chinese Journal of Catalysis , 编辑部邮箱 ,2008年03期
  • 【分类号】O643.32
  • 【被引频次】9
  • 【下载频次】370
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