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1,4-di[4-(7-hydroxy-7-methylocta-1,3,5-triynyl)phenyl]-buta-1,3-diyne | 1191093-47-6

中文名称
——
中文别名
——
英文名称
1,4-di[4-(7-hydroxy-7-methylocta-1,3,5-triynyl)phenyl]-buta-1,3-diyne
英文别名
8-[4-[4-[4-(7-Hydroxy-7-methylocta-1,3,5-triynyl)phenyl]buta-1,3-diynyl]phenyl]-2-methylocta-3,5,7-triyn-2-ol
1,4-di[4-(7-hydroxy-7-methylocta-1,3,5-triynyl)phenyl]-buta-1,3-diyne化学式
CAS
1191093-47-6
化学式
C34H22O2
mdl
——
分子量
462.547
InChiKey
ZZYBGKPUZOWJAN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    6.1
  • 重原子数:
    36
  • 可旋转键数:
    11
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    1,4-di[4-((E)-3-tert-butyldiphenylsilyl-4-chloro-7-hydroxy-7-methyl-oct-3-ene-1,5-diynyl)-phenyl]-buta-1,3-diyne 在 四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 以76%的产率得到1,4-di[4-(7-hydroxy-7-methylocta-1,3,5-triynyl)phenyl]-buta-1,3-diyne
    参考文献:
    名称:
    Synthesis of Hybrid Masked Triyne−Phenylene Axial Rods Containing (E)-β-Chlorovinylsilanes in the π-Conjugated Framework
    摘要:
    A two-directional synthesis of a masked hexayne 7, in which two beta-chlorovinylsilanes protect two of the internal alkynes, is reported. The key step involves the Pd-catalyzed oxidative dimerization of alkyne 10 to provide diyne 12, which is elaborated into centrosymmetric masked hexayne 7 in four steps. Masked hexayne 7 is a constitutional isomer of masked hexayne 2, which has been used as a monomer unit for oligoyne assembly. Although masked hexayne 7 was not as convenient a building block as 2 for application in oligoyne assembly, one of its precursors, namely alkyne 10, could be used successfully in Sonogashira couplings, which allowed the incorporation of aromatic spacers and the formation of hybrid masked triyne-phenylenes 20 and 28. Compounds 20 and 28 both contain removable end-groups, which will permit their application as building blocks for the assembly of classes of long-chain, pi-conjugated rod-like molecules. Rod-like molecule 34, which possesses a similar conjugated scaffold as 28, was also prepared by using a similar Strategy. Treatment of 34 with TBAF effected a 2-fold dechlorosilylation to provide a rigid rod molecule 35 in which two phenylene units interrupt an octayne scaffold.
    DOI:
    10.1021/jo901766p
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