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串联反应合成氟磺酸联苯酚酯

本站小编 Free考研考试/2022-02-14

摘要/Abstract



发展了一个以溴代苯酚为原料通过串联反应制备氟磺酸联苯酚酯的反应体系.该体系以钯碳为催化剂,无水碳酸钾为碱,乙醇水溶液为溶剂,室温下进行Suzuki反应后,通入硫酰氟气体,最终得到氟磺酸联苯酚酯.反应过程中无需分离中间体,无需加入有机膦配体及氮气保护反应,操作简便,反应条件温和,官能团底物兼容性好,产品分离收率最高达92.6%;此外,钯碳催化剂可回收使用三次几乎不失去活性.
关键词: 苯酚, 氟磺酸联苯酚酯, Suzuki反应, 串联反应, 钯碳
The one-pot tandem protocol for the preparation of biaryl fluorosulfates from bromo phenols was developed. Using Pd/C as catalyst, K2CO3 as base and aqueous ethanol as solvent, the Suzuki reaction was carried out at room temperature, then SO2F2 gas was added to the mixture to afford biaryl fluorosulfates product. The intermediate was not isolated, and phosphine ligand and nitrogen protection were not required during the reaction, which made the protocol more convenient to operate. The one-pot protocol could tolerate a range of functional groups and provided a highest product yield up to 97.2% at room temperature. Furthermore, Pd/C catalyst could be recycled and reused three times without significant loss of catalytic activity
Key words: phenol, baryl fluorosulfates, Suzuki reaction, one-pot reaction, Pd/C


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