6,13-bis(trimethylsilyl)-5,14-dihydropentacene | 1234434-11-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 并四苯
• 英文名称: 6,13-bis(trimethylsilyl)-5,14-dihydropentacene
• 英文别名: trimethyl-(13-trimethylsilyl-5,14-dihydropentacen-6-yl)silane
• CAS: 1234434-11-7
• 化学式: C₂₈H₃₂Si₂
• 分子量: 424.733
• InChiKey: LBLMZTVSHMNSJV-UHFFFAOYSA-N

物化性质

• 沸点：
  486.9±45.0 °C(Predicted)
• 密度：
  1.06±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6.58
• 重原子数：
  30
• 可旋转键数：
  2
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  6,13-bis(trimethylsilyl)-5,14-dihydropentacene 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide 、 一氯化碘 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 9.0h， 生成 6,13-bis(trimethylsilylethynyl)-5,14-dihydropentacene
  参考文献：
  名称：

  Application of Zirconacyclopentadienes (Metalla-heterocycles) and Cross-Coupling for the Convenient Preparative Method of 6,13-Disubstituted Pentacene

  摘要：

  Iodination of zirconacyclopentadiene derivative gave diiododiene derivative. The product was lithiated with t-BuLi and treated with diiodonaphthalene successively to afford 6,13-bis(trimethylsilyl)-5,14-dihydropentacene. A 6,13-diiodo-5,14-dihydropentacene was synthesized by iodination of 6,13-bis(trimethylsilyl)-5,14-dihydropentacene with ICl. This diiododihydropentacene was used for the introduction of substituent at 6 and 13 positions by the cross-coupling reactions with Pd catalyst. After aromatization by a combination of DDQ and gamma-terpinene or triethylamine, 6,13-disubstituted pentacene derivatives were synthesized.

  DOI：

  10.3987/com-12-s(n)130
• 作为产物：
  描述：

  2,3-bis[1-iodo1-trimethylsilylmethylene]-1,2,3,4-tetrahydronaphthalene 、 2,3-二碘萘 在 叔丁基锂 、 N,N-二甲基丙烯基脲 、 copper(l) chloride 作用下， 以 四氢呋喃 、 正戊烷 为溶剂， 反应 5.0h， 以40%的产率得到6,13-bis(trimethylsilyl)-5,14-dihydropentacene
  参考文献：
  名称：

  6,13-​​双（三甲基甲硅烷基）并五苯的制备及并五苯并二环-Diels-Alder加成物的形成

  摘要：

  通过双环二硫代丁二烯与二碘代萘的偶合反应合成6,13-​​双（三甲基甲硅烷基）并五苯。6,13-​​双（三甲基甲硅烷基）并五苯与亲二烯物的Diels-Alder反应得到相应的第二环加合物。消除两个甲硅烷基基团得到母并五苯的二环Diels-Alder加合物。

  DOI：

  10.1021/jo101774d

文献信息

• Lithiation of palladated dihydropentacene: a new route for the introduction of substituents from both of electrophiles and nucleophiles to pentacene
  作者：Yanqing Wang、Kiyohiko Nakajima、Zhiyi Song、Tamotsu Takahashi

  DOI：10.1039/c7cc09535j

  日期：——

  Dibromodihydropentacene compound 1 was palladated and then lithiated to give a lithiated-palladated intermediate. Both of the lithium moiety and the palladium complex moiety on dihydropentacene unexpectedly survived in the solution. The Li and Pd moieties reacted with electrophiles and nucleophiles respectively to give the substituted dihydropentacene products. Aromatization of these dihydropentacenes

  将二溴二氢并五苯化合物1钯化，然后锂化，得到锂化钯化的中间体。二氢并五苯上的锂部分和钯配合物部分均出乎意料地在溶液中存活。Li和Pd部分分别与亲电试剂和亲核试剂反应，得到取代的二氢并五苯产物。这些二氢戊烯的芳构化得到取代的并五苯衍生物。
• 6,13-DIHALOGEN-5,14-DIHYDROPENTACENE DERIVATIVE AND METHOD FOR PRODUCING 6,13-SUBSTITUTED-5,14-DIHYDROPENTACENE DERIVATIVE USING SAME
  申请人：Takahashi Tamotsu

  公开号：US20130079530A1

  公开（公告）日：2013-03-28

  The present invention provides a 6,13-dihalogen-5,14-dihydropentacene derivative and a method for production thereof. Compounds (b) and (c) are reacted through cross-coupling reaction in the presence of a metal compound and a lithiating agent to synthesize compound (d), which is then halogenated to thereby obtain a 6,13-dihalogen-5,14-dihydropentacene derivative (compound (e)). [wherein X 1 and X 2 are each a halogen atom, and R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are each a hydrogen atom, an optionally substituted C 1 -C 20 hydrocarbon group, etc.]

  本发明提供了一种6，13-二卤代-5，14-二氢戊五烯衍生物及其生产方法。通过在金属化合物和锂化剂的存在下，将化合物（b）和（c）通过交叉偶联反应反应，合成化合物（d），然后通过卤代反应获得6，13-二卤代-5，14-二氢戊五烯衍生物（化合物（e））。[其中X1和X2均为卤素原子，R1、R2、R3、R4、R5、R6、R7、R8、R9和R10均为氢原子、可选的取代的C1-C20碳氢基团等]
• 6,13-dihalogen-5,14-dihydropentacene derivative and method for producing 6,13-substituted-5,14-dihydropentacene derivative using same
  申请人：Takahashi Tamotsu

  公开号：US08785671B2

  公开（公告）日：2014-07-22

  The present invention provides a 6,13-dihalogen-5,14-dihydropentacene derivative and a method for production thereof. Compounds (b) and (c) are reacted through cross-coupling reaction in the presence of a metal compound and a lithiating agent to synthesize compound (d), which is then halogenated to thereby obtain a 6,13-dihalogen-5,14-dihydropentacene derivative (compound (e)). [wherein X1 and X2 are each a halogen atom, and R1, R2, R3, R4, R5, R6, R7, R8, R9 and R10 are each a hydrogen atom, an optionally substituted C1-C20 hydrocarbon group, etc.]

  本发明提供了一种6,13-二卤代-5,14-二氢基五环十二烯衍生物及其制备方法。通过在金属化合物和锂化剂的存在下，使化合物（b）和（c）通过交叉偶联反应反应，合成化合物（d），然后进行卤代反应，从而获得6,13-二卤代-5,14-二氢基五环十二烯衍生物（化合物（e））。[其中X1和X2均为卤素原子，R1、R2、R3、R4、R5、R6、R7、R8、R9和R10均为氢原子，可选地取代的C1-C20烃基等]。
• Preparation of 6,13-Bis(trimethylsilyl)pentacene and Formation of Second-Ring Diels−Alder Adduct of Pentacene
  作者：Zhiying Jia、Shi Li、Kiyohiko Nakajima、Ken-ichiro Kanno、Tamotsu Takahashi

  DOI：10.1021/jo101774d

  日期：2011.1.7

  synthesized by a coupling reaction of bicyclic dilithiobutadiene with diiodonaphthalene followed by aromatization. Diels−Alder reaction of 6,13-bis(trimethylsilyl)pentacene with dienophiles afforded the corresponding second-ring adducts. Elimination of two silyl groups gave the second-ring Diels−Alder adducts of parent pentacene.

  通过双环二硫代丁二烯与二碘代萘的偶合反应合成6,13-​​双（三甲基甲硅烷基）并五苯。6,13-​​双（三甲基甲硅烷基）并五苯与亲二烯物的Diels-Alder反应得到相应的第二环加合物。消除两个甲硅烷基基团得到母并五苯的二环Diels-Alder加合物。
• Application of Zirconacyclopentadienes (Metalla-heterocycles) and Cross-Coupling for the Convenient Preparative Method of 6,13-Disubstituted Pentacene
  作者：Tamotsu Takahashi、Zhiying Jia、Shi Li、Kiyohiko Nakajima、Ken-ichiro Kanno、Zhiyi Song

  DOI：10.3987/com-12-s(n)130

  日期：——

  Iodination of zirconacyclopentadiene derivative gave diiododiene derivative. The product was lithiated with t-BuLi and treated with diiodonaphthalene successively to afford 6,13-bis(trimethylsilyl)-5,14-dihydropentacene. A 6,13-diiodo-5,14-dihydropentacene was synthesized by iodination of 6,13-bis(trimethylsilyl)-5,14-dihydropentacene with ICl. This diiododihydropentacene was used for the introduction of substituent at 6 and 13 positions by the cross-coupling reactions with Pd catalyst. After aromatization by a combination of DDQ and gamma-terpinene or triethylamine, 6,13-disubstituted pentacene derivatives were synthesized.