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作 者:吴其旭 王俊雅 罗云飞 Wu Qixu;Wang Junya;Luo Yunfei(School of Chemistry and Chemical Engineering,Hefei University of Technology,Hefei,Anhui 230009,China)
机构地区:[1]合肥工业大学化学与化工学院,安徽合肥230009
出 处:《化学世界》2021年第5期290-294,共5页Chemical World
摘 要:将Pd(OAc)_(2)与2-二苯膦基苯甲醛络合,再与甲醛、尿素缩合反应制备脲醛树脂,得到固载钯催化剂。用固载钯催化剂进行一系列芳基硼酸与芳基卤代物的Suzuki耦联反应。研究结果表明,固载钯催化剂在温和的反应条件下催化合成联苯类化合物,收率>86%,合成的固载钯催化剂具有良好的重复利用性。Pd(OAc)_(2) was complexed with 2-(diphenylphosphino)benzaldehyde, and then condensed with formaldehyde and urea to prepare urea formaldehyde resin for the supported catalyst of palladium. A series of Suzuki coupling reactions between aryl boric acid and aryl halide were performed using the obtained supported catalyst. The results showed that the immobilized catalyst could afford bi-aryl compounds efficiently under mild reaction conditions and with yields over 86%. This resin supported palladium catalyst has also showed good reusability.
关 键 词:脲醛树脂 PD(OAC)2 2-二苯膦基苯甲醛 Suzuki耦联反应
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