bis(2-thienyl)diphenylsilane | 18676-80-7

• 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: bis(2-thienyl)diphenylsilane
• 英文别名: diphenyl(di-2-thienyl)silane；diphenyl-di-[2]thienyl-silane；Diphenyl-di-[2]thienyl-silan；Diphenyldi(thiophen-2-yl)silane；diphenyl(dithiophen-2-yl)silane
• CAS: 18676-80-7
• 化学式: C₂₀H₁₆S₂Si
• 分子量: 348.565
• InChiKey: GMIUAOFYMAZWDL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.19
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  56.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  bis(2-thienyl)diphenylsilane 在 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 以86%的产率得到二苯基二羟基硅烷
  参考文献：
  名称：

  Bis(2-thienyl)silanes: new, versatile precursors to arylsilanediols

  摘要：

  Silanediols have been shown to be effective bioisosteres for the hydrated carbonyl group. Current methods for the formation of silanediols place a number of constraints on how and where this functionality may be used. A range of arylsilanes that would allow both the formation of arylsilanediols and that are also compatible with multi-step synthetic routes, have been investigated as possible precursors to silanediols. Through this study bis(2-furyl)silanes and, in particular, bis(2-thienyl)si lanes have been identified as practical precursors to arylsilanediols. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.03.095
• 作为产物：
  描述：

  2-噻吩基锂 、 二苯二氯硅烷 以 四氢呋喃 为溶剂， 反应 18.0h， 以84%的产率得到bis(2-thienyl)diphenylsilane
  参考文献：
  名称：

  Bis(2-thienyl)silanes: new, versatile precursors to arylsilanediols

  摘要：

  Silanediols have been shown to be effective bioisosteres for the hydrated carbonyl group. Current methods for the formation of silanediols place a number of constraints on how and where this functionality may be used. A range of arylsilanes that would allow both the formation of arylsilanediols and that are also compatible with multi-step synthetic routes, have been investigated as possible precursors to silanediols. Through this study bis(2-furyl)silanes and, in particular, bis(2-thienyl)si lanes have been identified as practical precursors to arylsilanediols. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.03.095

文献信息

• Integrated Palladium-Catalyzed Arylation of Heavier Group 14 Hydrides
  作者：Aldes Lesbani、Hitoshi Kondo、Yusuke Yabusaki、Misaki Nakai、Yoshinori Yamanoi、Hiroshi Nishihara

  DOI：10.1002/chem.201001437

  日期：2010.12.3

  A convenient procedure has been developed for the preparation of Group 14 compounds by integrated palladium‐catalyzed cross‐coupling of aromatic iodides with the corresponding Group 14 hydrides in the presence of a base. The reaction conditions can be applied to the cross‐coupling of tertiary, secondary, and primary Group 14 compounds. In most cases, the desired arylated products were obtained in synthetically

  在碱的存在下，通过钯催化的芳族碘化物与相应的14族氢化物的交叉偶联，已经开发出了一种方便的制备14族化合物的方法。该反应条件可用于第14组叔，仲和伯化合物的交叉偶联。在大多数情况下，所需的芳基化产物以合成有用的产率获得。即使在含OH，NH芳基碘的情况下2，CN或CO 2 R基团，具有良好的取得高产量的这些反应性官能团的耐受性进行的反应。这种方法的一个可能的应用是一个杀真菌二芳基（1的唯一合成ħ -1,2,4-三唑-1-基甲基）硅烷衍生物。
• Electrochemical synthesis of bis(2-thienyl) silanes, 2-thienylchlorosilanes, bis[5-(2-bromothienyl)]silanes, and 5-(2-bromothienyl) dimethylchlorosilane, precursors of poly[(silanylene)thiophene]s
  作者：Carole Moreau、Françoise Serein-Spirau、Michel Bordeau、Claude Biran、Jacques Dunoguès

  DOI：10.1016/0022-328x(96)06333-4

  日期：1996.9

  Bis(2-thienyl)silanes and bis[5-(2-bromothienyl)]silanes were synthesized by electrochemical reduction of monohalothiophenes (Br,Cl) and 2,5-dibromothiophene respectively in the presence of a dichlorosilane in THF or LME, using an undivided cell, a sacrificial Mg or Al anode, a constant current density and tetrabutylammonium bromide as the supporting electrolyte. In addition, when dichlorosilanes were

  通过在THF或LME中在二氯硅烷存在下分别通过单卤代噻吩（Br，Cl）和2,5-二溴噻吩的电化学还原反应，合成了双（2-噻吩基）硅烷和双[5-（2-溴噻吩基）]硅烷一个未分割的电池，一个牺牲性的Mg或Al阳极，一个恒定的电流密度和四丁基溴化铵作为支持电解质。另外，当大量使用二氯硅烷时，卤代噻吩仅进行单偶联反应，选择性地导致噻吩基氯硅烷，这揭示了电化学方法的多功能性。
• Spialter; Harris, <1959> 1, 4
  作者：Spialter、Harris

  DOI：——

  日期：——