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3-[(2-Phenylmethoxyphenyl)methyl]-1,2,4-trioxolane | 1373139-17-3

中文名称
——
中文别名
——
英文名称
3-[(2-Phenylmethoxyphenyl)methyl]-1,2,4-trioxolane
英文别名
——
3-[(2-Phenylmethoxyphenyl)methyl]-1,2,4-trioxolane化学式
CAS
1373139-17-3
化学式
C16H16O4
mdl
——
分子量
272.301
InChiKey
QGSSHKSBGSOWGB-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:
    386.3±37.0 °C(Predicted)
  • 密度:
    1.211±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    20
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    36.9
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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:
    3-[(2-Phenylmethoxyphenyl)methyl]-1,2,4-trioxolane2,4,6-三甲基吡啶二氯二茂钛三甲基氯硅烷 作用下, 以 四氢呋喃 为溶剂, 反应 3.0h, 以99%的产率得到1-Phenylmethoxy-2-[2-(2-phenylmethoxyphenyl)ethyl]benzene
    参考文献:
    名称:
    Ti-Catalyzed Homolytic Opening of Ozonides: A Sustainable C–C Bond-Forming Reaction
    摘要:
    The unprecedented homolytic opening of ozonides promoted and catalyzed by titanocene(III) is reported. This novel reaction proceeds at room temperature under neutral, mild conditions compatible with many functional groups and provides carbon radicals suitable to form C-C bonds via both homocoupling and cross-coupling processes. The procedure has been advantageously exploited for the straightforward synthesis of the natural product brittonin A.
    DOI:
    10.1021/jo300344a
  • 作为产物:
    描述:
    1-allyl-2-(benzyloxy)benzene臭氧 作用下, 以 二氯甲烷 为溶剂, 以73%的产率得到3-[(2-Phenylmethoxyphenyl)methyl]-1,2,4-trioxolane
    参考文献:
    名称:
    Ti-Catalyzed Homolytic Opening of Ozonides: A Sustainable C–C Bond-Forming Reaction
    摘要:
    The unprecedented homolytic opening of ozonides promoted and catalyzed by titanocene(III) is reported. This novel reaction proceeds at room temperature under neutral, mild conditions compatible with many functional groups and provides carbon radicals suitable to form C-C bonds via both homocoupling and cross-coupling processes. The procedure has been advantageously exploited for the straightforward synthesis of the natural product brittonin A.
    DOI:
    10.1021/jo300344a
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文献信息

  • Ti-Catalyzed Homolytic Opening of Ozonides: A Sustainable C–C Bond-Forming Reaction
    作者:Antonio Rosales、Juan Muñoz-Bascón、Cristóbal López-Sánchez、Míriam Álvarez-Corral、Manuel Muñoz-Dorado、Ignacio Rodríguez-García、J. Enrique Oltra
    DOI:10.1021/jo300344a
    日期:2012.4.20
    The unprecedented homolytic opening of ozonides promoted and catalyzed by titanocene(III) is reported. This novel reaction proceeds at room temperature under neutral, mild conditions compatible with many functional groups and provides carbon radicals suitable to form C-C bonds via both homocoupling and cross-coupling processes. The procedure has been advantageously exploited for the straightforward synthesis of the natural product brittonin A.
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