CAS: 912350-01-7; Potassium [4-(Phenylamino-1-Carbonyl)-Phenyl]Trifluoroborate

该化合物是一种有机三氟乙烷化合物,通常在苏祖基-米亚乌拉的交错反应中用作稳定的碳酸酸代谢器,其三氟乙酸混合物可以稳定地防止子球和氧化,改进处理和储存与常规碳酸相比.苯氨基碳基子成分引入了额外的功能,使其成为制药和材料科学应用的多种中间体.这种化合物因其可预见地回动性及与不同反应条件的兼容性,在可受控的选择性转化中特别有用.其晶体特性可以确保高纯度,便于合成工作流程的再生结果.

结构式图片

欧盟法规

C&L通报

合成工艺路线路线简述

  • 374564-35-9 = 912350-01-7
    反应条件:1.1 Reagents: Butyllithium Solvents: Tetrahydrofuran; 1 H,-78 °C1.2 10 Min,-78 °C; -78 °C -> Rt; 30 Min,Rt1.3 Reagents: Potassium Bifluoride Solvents: Water; 10 Min,Rt
    标题:Linchpin Synthons: Metalation Of Aryl Bromides Bearing A Potassium Trifluoroborate Moiety
    作者:Molander,Gary A.; Et Al
    参考文献:Journal Of Organic Chemistry 日期:2006 卷标:71(19) 页码:7491-7493
📜异氰酸苯酯,4-溴苯基三氟硼酸钾置于正丁基锂,Potassium Hydrogen Bifluoride体系中,用 四氢呋喃 作为反应溶剂,化学反应 1.92H,以68%的收率获得产物4-(苯基胺基羰基)苯基三氟硼酸钾
参考文献:Linchpin Synthons: Metalation Of Aryl Bromides Bearing A Potassium Trifluoroborate Moiety
标题:Linchpin Synthons: Metalation Of Aryl Bromides Bearing A Potassium Trifluoroborate Moiety
摘要:Aryl Bromides Bearing A Potassium Trifluoroborate Moiety Were Subjected To Lithium-Halogen Exchange At Low Temperature Using A Variety Of Alkyllithium Reagents. A Number Of Different Electrophiles Were Evaluated In Their Reactions With The Aryllithiums Produced Therein. Under Carefully Optimized Conditions,Potassium Bromophenyl Trifluoroborates Afforded Good To Excellent Yields Of The Corresponding Alcohols (64-94% Isolated Yield) When Aldehydes Or Ketones Were Used As The Electophilic Partner. Esters Were Unfortunately Found To Be Unreactive.
DOI:10.1021/jo061324U

海关参考信息

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

合成参考文献


参考文献:10.1055/s-2006-955611
摘要:Molander G, Ellis N. Metallation of Aryl Bromides Bearing a Potassium Trifluoroborate Moiety. Synfacts. 2006 Dec;2006(12):1269. doi: 10.1055/s-2006-955611.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知