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3,6,9,12,16,19,22,26-Octaoxa-13,25-diazatricyclo[22.2.1.111,14]octacosa-1(27),11(28),13,24-tetraene | 203740-54-9

中文名称
——
中文别名
——
英文名称
3,6,9,12,16,19,22,26-Octaoxa-13,25-diazatricyclo[22.2.1.111,14]octacosa-1(27),11(28),13,24-tetraene
英文别名
——
3,6,9,12,16,19,22,26-Octaoxa-13,25-diazatricyclo[22.2.1.111,14]octacosa-1(27),11(28),13,24-tetraene化学式
CAS
203740-54-9
化学式
C18H26N2O8
mdl
——
分子量
398.413
InChiKey
UGKTXMLWLCWFJW-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

物化性质

  • 沸点:
    640.3±50.0 °C(Predicted)
  • 密度:
    1.144±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.3
  • 重原子数:
    28
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    107
  • 氢给体数:
    0
  • 氢受体数:
    10

反应信息

  • 作为反应物:
    描述:
    3,6,9,12,16,19,22,26-Octaoxa-13,25-diazatricyclo[22.2.1.111,14]octacosa-1(27),11(28),13,24-tetraene ion-exchange resin Dowex XW-50 、 氢气 作用下, 以 甲醇 为溶剂, 反应 8.0h, 生成 3,5,15,17-tetraoxo-1,7,10,13,19,22-hexaoxacyclotetracosane
    参考文献:
    名称:
    Organic metal-complexes. XXI. Synthesis and structure of 3,5,15,17-tetraoxo-1,7,10,13,19,22-hexaoxa-cyclotetracosane and 2,12,14,24-tetraoxo-4,7,10,16,19,22-hexaoxa-25-mercurato-bicyclo[11.11.1]pentacosane
    摘要:
    A new synthesis of the title crown via isoxazolo crown ether 7 and macrocyclic bis-peneaminoketone 10 is described. 7 can be synthesized in 14% yield by a non-template double-[3+2] cycloaddition of dinitrileoxide 5 prepared in situ from dinitropolyether 19 by dehydration with Ph-NCO and alkyne 6. The compounds 16, 17 and 18 are synthesized by the same synthetic strategy. Comparable IR and H-1 NMR spectroscopic data of macrocyclic and non-cyclic compounds show, that macrocyclic conformation stabilizing effects can be ruled out. The structures of the macrocycles 1, 7, 10 and that of the Hg(II)-complex 25, synthesized by reaction of 1 with Hg(OAc)(2) were established by single-crystal X-ray structure analyses. Both inter-and intramolecular hydrogen bonds are observed for the macrocyclic bis-beta-eneaminoketone 10, whereas only intramolecular hydrogen bonds are formed by 1. In the Hg(II)-complex of 1 the mercury is bonded to two methylene groups. C-Hg-C is almost linear [177(1)degrees], the mean Hg-C distance amounts to 215(1) pm. In addition to the Hg-C bonds, each Hg makes a short contact to a carbonyl oxygen in a neighbouring molecule in the plane perpendicular to the C-Hg-C axis [Hg(1)-O(1) = 279(1) pm, Hg(2)-O(5)= 284(1) pm].
    DOI:
    10.1002/prac.19983400207
  • 作为产物:
    参考文献:
    名称:
    Organic metal-complexes. XXI. Synthesis and structure of 3,5,15,17-tetraoxo-1,7,10,13,19,22-hexaoxa-cyclotetracosane and 2,12,14,24-tetraoxo-4,7,10,16,19,22-hexaoxa-25-mercurato-bicyclo[11.11.1]pentacosane
    摘要:
    A new synthesis of the title crown via isoxazolo crown ether 7 and macrocyclic bis-peneaminoketone 10 is described. 7 can be synthesized in 14% yield by a non-template double-[3+2] cycloaddition of dinitrileoxide 5 prepared in situ from dinitropolyether 19 by dehydration with Ph-NCO and alkyne 6. The compounds 16, 17 and 18 are synthesized by the same synthetic strategy. Comparable IR and H-1 NMR spectroscopic data of macrocyclic and non-cyclic compounds show, that macrocyclic conformation stabilizing effects can be ruled out. The structures of the macrocycles 1, 7, 10 and that of the Hg(II)-complex 25, synthesized by reaction of 1 with Hg(OAc)(2) were established by single-crystal X-ray structure analyses. Both inter-and intramolecular hydrogen bonds are observed for the macrocyclic bis-beta-eneaminoketone 10, whereas only intramolecular hydrogen bonds are formed by 1. In the Hg(II)-complex of 1 the mercury is bonded to two methylene groups. C-Hg-C is almost linear [177(1)degrees], the mean Hg-C distance amounts to 215(1) pm. In addition to the Hg-C bonds, each Hg makes a short contact to a carbonyl oxygen in a neighbouring molecule in the plane perpendicular to the C-Hg-C axis [Hg(1)-O(1) = 279(1) pm, Hg(2)-O(5)= 284(1) pm].
    DOI:
    10.1002/prac.19983400207
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