催化学报 ›› 2009, Vol. 30 ›› Issue (3): 242-246.

• 研究论文 • 上一篇    下一篇

离子液体介质中钌膦配合物催化的喹啉加氢反应

李强1, 张瑞敏1, 周丽梅1,2, 付海燕1, 陈华1, 李贤均1   

  1. 1四川大学化学学院有机金属络合催化研究所, 绿色化学及技术教育部重点实验室, 四川成都610064; 2西华师范大学化学化工学院, 四川南充637002
  • 收稿日期:2009-03-25 出版日期:2009-03-25 发布日期:2012-12-19

Hydrogenation of Quinoline Catalyzed by Ruthenium Phosphine Complex in Ionic Liquids

LI Qiang1, ZHANG Ruimin1, ZHOU Limei1,2, FU Haiyan1, CHEN Hua1,*, LI Xianjun1   

  1. 1Institute of Homogeneous Catalysis, College of Chemistry, Key Laboratory of Green Chemistry and Technology of Ministry of Education, Sichuan University, Chengdu 610064, Sichuan, China; 2Department of Chemistry and Chemical Engineering, West China Normal University, Nanchong 637002, Sichuan, China
  • Received:2009-03-25 Online:2009-03-25 Published:2012-12-19

摘要: 首次在亲水性离子液体[Rmim][p-CH3C6H4SO3](1-烷基-3-甲基咪唑对甲苯磺酸盐, R = 甲基、乙基、正丁基、正己基和正辛基)中, 以水溶性的[RuCl2(TPPTS)2]2 (TPPTS: 间磺酸钠基三苯基膦)为催化剂, 分别考察了温度、压力、不同的离子液体、水和碘的加入等因素对喹啉加氢反应的影响. 在100 oC和氢气压力为3.0 MPa时, 喹啉加氢生成1,2,3,4-四氢喹啉的选择性超过99%, 转化率达到95.3%. 利用环己烷萃取反应产物, 即可实现催化剂与产物的分离, 催化剂循环使用6次后反应的转化率仍可达86.0%.

关键词: 钌膦配合物, 喹啉, 加氢, 离子液体, 两相催化, 1, 2, 3, 4-四氢喹啉

Abstract: The catalyst [RuCl2(TPPTS)2]2 was used in the regioselective hydrogenation of quinoline in [Rmim][p-CH3C6H4SO3] with high conversion and selectivity. The products can be easily separated from the catalyst immobilized in ionic liquids by simple extraction with cycohexane. The conversion reached 86.0% when the catalyst was reused 6 times.

Key words: ruthenium phosphine complex, quinoline, hydrogenation, ionic liquid, biphasic catalysis, 1, 2, 3, 4-tetrahydroquinoline