2-(4,4,4-trifluorobutyl)isoindoline-1,3-dione | 453559-01-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异吲哚及其衍生物
• 英文名称: 2-(4,4,4-trifluorobutyl)isoindoline-1,3-dione
• 英文别名: 2-(4,4,4-Trifluorobutyl)isoindole-1,3-dione；2-(4,4,4-trifluorobutyl)isoindole-1,3-dione
• CAS: 453559-01-8
• 化学式: C₁₂H₁₀F₃NO₂
• 分子量: 257.212
• InChiKey: MVCJSQOCMFLZND-UHFFFAOYSA-N

物化性质

• 沸点：
  303.1±42.0 °C(Predicted)
• 密度：
  1.356±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  37.4
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  S-(1-(1,3-dioxoisoindolin-2-yl)-4,4,4-trifluorobutan-2-yl) O-octadecyl carbonodithioate 在 磷酸 、 三乙胺 、 偶氮二异丁腈 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 1.25h， 以85%的产率得到2-(4,4,4-trifluorobutyl)isoindoline-1,3-dione
  参考文献：
  名称：

  A Convenient Metal-Free Reagent for the Generation and Capture of Trifluoromethanethiol

  摘要：

  0-Octadecyl-S-trifluorothiolcarbonate is a cheap and storable crystalline source of trifluoromethanethiol that can be prepared in two steps on a multigram scale from trifluoroacetic anhydride and sodium 0-octadecyl-dithiocarbonate (xanthate). It reacts directly with gramines or with alpha-bromoketones and -esters in the presence of KF and pyrrolidine to give the corresponding trifluoromethyl sulfides in generally high yield.

  DOI：

  10.1021/ol403038f

文献信息

• Copper-Catalyzed Reductive Trifluoromethylation of Alkyl Iodides with Togni’s Reagent
  作者：Yanchi Chen、Guobin Ma、Hegui Gong

  DOI：10.1021/acs.orglett.8b02005

  日期：2018.8.3

  This work illustrates a reductive cross-electrophile coupling protocol for trifluoromethylation of alkyl iodides under Cu-catalyzed/Ni-promoted reaction conditions. The use of diboron esters as the terminal reductant allows the effective generation of the alkyl–CF3 products with excellent functional group tolerance and broad substrate scope. A mechanism involving a reaction of alkyl–Cu with Togni’s

  这项工作说明了在Cu催化/ Ni促进的反应条件下烷基碘的三氟甲基化的还原性交亲电子偶联方案。使用二硼酸酯作为末端还原剂可以有效生成具有出色的官能团耐受性和广泛的底物范围的烷基-CF 3产物。提出了一种涉及烷基铜与Togni试剂反应的机理。
• Catalytic Hydrotrifluoromethylation of Unactivated Alkenes
  作者：Satoshi Mizuta、Stefan Verhoog、Keary M. Engle、Tanatorn Khotavivattana、Miriam O’Duill、Katherine Wheelhouse、Gerasimos Rassias、Maurice Médebielle、Véronique Gouverneur

  DOI：10.1021/ja401022x

  日期：2013.2.20

  A visible-light-mediated hydrotrifluoromethylation of unactivated alkenes that uses the Umemoto reagent as the CF(3) source and MeOH as the reductant is disclosed. This effective transformation operates at room temperature in the presence of 5 mol % Ru(bpy)(3)Cl(2); the process is characterized by its operational simplicity and functional group tolerance.

  公开了使用 Umemoto 试剂作为 CF(3) 源和 MeOH 作为还原剂的未活化烯烃的可见光介导的氢三氟甲基化。这种有效的转变在室温下在 5 mol % Ru(bpy)(3)Cl(2) 存在下进行；该过程的特点是其操作简单和官能团耐受性。
• Trifluoromethylation of Alkyl Radicals in Aqueous Solution
  作者：Haigen Shen、Zhonglin Liu、Pei Zhang、Xinqiang Tan、Zhenzhen Zhang、Chaozhong Li

  DOI：10.1021/jacs.7b06044

  日期：2017.7.26

  The copper-mediated trifluoromethylation of alkyl radicals is described. The combination of Et3SiH and K2S2O8 initiates the radical reactions of alkyl bromides or iodides with BPyCu(CF3)3 (BPy = 2,2'-bipyridine) in aqueous acetone at room temperature to afford the corresponding trifluoromethylation products in good yield. The protocol is applicable to various primary and secondary alkyl halides and

  描述了铜介导的烷基三氟甲基化。Et3SiH 和 K2S2O8 的组合在室温下在丙酮水溶液中引发烷基溴化物或碘化物与 BPyCu(CF3)3（BPy = 2,2'-联吡啶）的自由基反应，以良好的收率提供相应的三氟甲基化产物。该协议适用于各种一级和二级烷基卤化物，并具有广泛的官能团兼容性。提出了一种涉及三氟甲基从 Cu(II)-CF3 中间体转移到烷基自由基的机制。
• Copper-catalyzed trifluoromethylation of organic zinc reagents with an electrophilic trifluoromethylating reagent
  作者：Chang-Sheng Wang、Haoyang Wang、Cheng Yao

  DOI：10.1039/c5ra02279g

  日期：——

  A copper-catalyzed trifluoromethylation of aryl, vinyl and alkyl zinc reagents with Togni's reagent was described. Mechanistic studies indicated that the aryl group is initially transferred from the zinc reagent to hypervalent iodine to form a tri-substituted hypervalent iodine intermediate. Consequent reductive-elimination via a concerted bond-forming step and/or radical pathway from this intermediate

  描述了用Togni试剂进行铜催化的芳基，乙烯基和烷基锌试剂的三氟甲基化。机理研究表明，芳基最初从锌试剂转移到高价碘上，形成三取代的高价碘中间体。因此，通过该中间体的协同键形成步骤和/或自由基途径的还原消除作用产生了三氟甲基化的芳烃。
• Diboron-Mediated Rhodium-Catalysed Transfer Hydrogenation of Alkenes and Carbonyls
  作者：Xiao Lin、Yuhan Wang、Yan Hu、Wanjiang Zhu、Xiaowei Dou

  DOI：10.1002/ejoc.202000049

  日期：2020.2.28

  A diboron‐mediated rhodium‐catalysed transfer hydrogenation system using water as the hydrogen donor is developed. The new system features broad substrate scope, good functional group tolerance, and controllable chemoselectivity. This rhodium‐based catalytic system provides a new tool for transfer hydrogenation.

  开发了一种以水为氢供体的二硼介导的铑催化的转移加氢系统。新系统具有广泛的底物范围，良好的官能团耐受性和可控的化学选择性。这种基于铑的催化系统为转移加氢提供了新的工具。