(4,4,4-trifluorobut-2-yn-1-yl)benzene | 1361988-25-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (4,4,4-trifluorobut-2-yn-1-yl)benzene
• 英文别名: 1,1,1-Trifluoro-4-phenyl-2-butyne；4,4,4-trifluorobut-2-ynylbenzene
• CAS: 1361988-25-1
• 化学式: C₁₀H₇F₃
• 分子量: 184.161
• InChiKey: SOZIUAZTTVVOOB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  3-苯-1-丙炔 在 叔丁基过氧化氢 、 正丁基锂 、 碳酸氢钠 、 copper(l) chloride 作用下， 以 四氢呋喃 、 甲醇 、 正己烷 、 二氯甲烷 、 水 为溶剂， 反应 5.0h， 生成 (4,4,4-trifluorobut-2-yn-1-yl)benzene
  参考文献：
  名称：

  Copper-mediated trifluoromethylation of potassium alkynyltrifluoroborates with Langlois' reagent

  摘要：

  Synthesis of trifluoromethylated acetylenes by copper-mediated trifluoromethylation of potassium alkynyltrifluoroborates with CF3 radicals generated from NaSO2CF3 and tert-butyl hydroperoxide (TBHP) is communicated. The trifluoromethylated acetylenes were obtained in good to moderate yields. The presented method tolerates a wide range of aromatic, heteroaromatic, and aliphatic potassium alkynyltrifluoroborates. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2014.02.005

文献信息

• Mild copper-catalyzed trifluoromethylation of terminal alkynes using an electrophilic trifluoromethylating reagent
  作者：Zhiqiang Weng、Huaifeng Li、Weiming He、Liang-Feng Yao、Jianwei Tan、Jinfa Chen、Yaofeng Yuan、Kuo-Wei Huang

  DOI：10.1016/j.tet.2011.12.085

  日期：2012.3

  A catalytic process for trifluoromethylation of terminal alkynes with Togni’s reagent has been developed, affording trifluoromethylated acetylenes in good to excellent yields. The reaction is conducted at room temperature and exhibits tolerance to a range of functional groups.

  已经开发出用Togni试剂催化末端炔烃的三氟甲基化的催化方法，从而以良好或优异的收率提供了三氟甲基化的乙炔。该反应在室温下进行，并且表现出对一定范围的官能团的耐受性。
• An Organocopper(III) Fluoride Triggering C−CF₃ Bond Formation
  作者：Daniel Joven‐Sancho、Andrea Echeverri、Nathalie Saffon‐Merceron、Julia Contreras‐García、Noel Nebra

  DOI：10.1002/anie.202319412

  日期：2024.3.11

  The first organocopper(III) fluoride, [PPh4][CuIII(CF3)3F] (2), has been isolated and authenticated. Despite its stability, 2 reacts with alkynylsilanes leading to industrially relevant trifluoromethylalkynes (RC≡CCF3). Mechanistic investigations, including the trapping of [PPh4][CuIII(CF3)3(C≡CPh)] (4a), validates the operability of a CuI/CuIII redox shuttle in oxidative C−C couplings occurring through

  第一种氟化有机铜(III) [PPh 4 ][Cu III (CF 3 ) 3 F] ( 2 ) 已被分离和鉴定。尽管具有稳定性， 2仍会与炔基硅烷发生反应，生成工业相关的三氟甲基炔烃 (RC≡CCF 3 )。机理研究，包括捕获 [PPh 4 ][Cu III (CF 3 ) 3 (CQICPh)] ( 4 a )，验证了 Cu I /Cu III氧化还原穿梭在氧化 C−C 偶联中的可操作性迄今为止难以捉摸的有机铜(III)氟化物。
• Cu-Catalyzed C–H Trifluoromethylation of 3-Arylprop-1-ynes for the Selective Construction of Allenic Csp²–CF₃ and Propargyl Csp³–CF₃ Bonds
  作者：Yun-Long Ji、Jia-Jia Luo、Jin-Hong Lin、Ji-Chang Xiao、Yu-Cheng Gu

  DOI：10.1021/acs.orglett.6b00120

  日期：2016.3.4

  A new method has been developed for the Cu-catalyzed C-H trifluoromethylation of 3-arylprop-1-ynes for the selective construction of allenic Csp(2)-CF3 and propargyl Csp(3)-CF3 bonds. The selective formation of allenic Csp(2)-CF3 and propargyl Csp(3)-CF3 bonds can be controlled by modifying the reaction conditions.