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trimethyl-[2-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-pentaoxabenzocyclopentadecen-15-yl)ethynyl]silane | 92710-92-4

中文名称
——
中文别名
——
英文名称
trimethyl-[2-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-pentaoxabenzocyclopentadecen-15-yl)ethynyl]silane
英文别名
4'-(2-Trimethylsilyleth-1-ynyl)benzo-15-crown-5;Trimethyl-[2-(2,5,8,11,14-pentaoxabicyclo[13.4.0]nonadeca-1(15),16,18-trien-17-yl)ethynyl]silane
trimethyl-[2-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-pentaoxabenzocyclopentadecen-15-yl)ethynyl]silane化学式
CAS
92710-92-4
化学式
C19H28O5Si
mdl
——
分子量
364.514
InChiKey
RXCNVQXWGKGBSB-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):
    2.74
  • 重原子数:
    25
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    46.2
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    trimethyl-[2-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-pentaoxabenzocyclopentadecen-15-yl)ethynyl]silane四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以89.5%的产率得到4'-乙炔基苯并15-冠-5
    参考文献:
    名称:
    The synthesis and structural characterization of the first bis(benzocrown ethers) with polyyne linkages †
    摘要:
    成功合成了双(苯并-15-冠醚-5)丁-1,3-二炔和双(苯并-15-冠醚-5)辛-1,3,5,7-四炔,并利用 X 射线晶体学对其进行了表征。此外,还研究了聚[双(苯并冠醚)二乙炔]的实验。
    DOI:
    10.1039/b001856m
  • 作为产物:
    描述:
    15-iodo-2,3,5,6,8,9,11,12-octahydrobenzo[b][1,4,7,10,13]pentaoxacyclopentadecane三甲基乙炔基硅 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide三乙胺 作用下, 以 为溶剂, 反应 2.5h, 以87%的产率得到trimethyl-[2-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-pentaoxabenzocyclopentadecen-15-yl)ethynyl]silane
    参考文献:
    名称:
    摘要:
    4 ' -Ethynylbenzo-12-crown-4 (8), 4 ' -ethynylbenzo-15-crown-5 (9), and 4 ' -ethynylbenzo-18-crown-6 (10) were synthesized by cross-coupling of the corresponding aryl iodides 1-3 with 2-methylbut-3-yn-2-ol (4a) followed by the retro-Favorsky cleavage of the resulting carbinols. Unlike the corresponding benzo-12-crown-4 derivative (5a), the cleavage of tertiary acetylenic, alcohols of benzo-15-crown-5 (6a) and benzo-18-crown-6 (7a) requires more than one molar equivalent of KOH. Aminoalkylation of crown ether 8 gives Mannich bases, independently of the reaction conditions and the nature of amine. The aminomethylation of acetylenic crown ethers 9 and 10 with paraform-piperidine (morpholine) in the presence of CuCl yields 1,4-disubstituted buta-1,3-diynes (19, 20) rather than Mannich bases.
    DOI:
    10.1023/a:1011367311643
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文献信息

  • The synthesis and structural characterization of the first bis(benzocrown ethers) with polyyne linkages †
    作者:Liang-Hui Lee、Vincent Lynch、Richard J. Lagow
    DOI:10.1039/b001856m
    日期:——
    Bis(benzo-15-crown-5)buta-1,3-diyne and bis(benzo-15-crown-5)octa-1,3,5,7-tetrayne were successfully synthesized and characterized by X-ray crystallography. Experiments with poly[bis(benzocrown ethers)diacetylene] were also studied.
    成功合成了双(苯并-15-冠醚-5)丁-1,3-二炔和双(苯并-15-冠醚-5)辛-1,3,5,7-四炔,并利用 X 射线晶体学对其进行了表征。此外,还研究了聚[双(苯并冠醚)二乙炔]的实验。
  • ——
    作者:S. V. Klyatskaya、E. V. Tretyakov、S. F. Vasilevsky
    DOI:10.1023/a:1011367311643
    日期:——
    4 ' -Ethynylbenzo-12-crown-4 (8), 4 ' -ethynylbenzo-15-crown-5 (9), and 4 ' -ethynylbenzo-18-crown-6 (10) were synthesized by cross-coupling of the corresponding aryl iodides 1-3 with 2-methylbut-3-yn-2-ol (4a) followed by the retro-Favorsky cleavage of the resulting carbinols. Unlike the corresponding benzo-12-crown-4 derivative (5a), the cleavage of tertiary acetylenic, alcohols of benzo-15-crown-5 (6a) and benzo-18-crown-6 (7a) requires more than one molar equivalent of KOH. Aminoalkylation of crown ether 8 gives Mannich bases, independently of the reaction conditions and the nature of amine. The aminomethylation of acetylenic crown ethers 9 and 10 with paraform-piperidine (morpholine) in the presence of CuCl yields 1,4-disubstituted buta-1,3-diynes (19, 20) rather than Mannich bases.
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