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bis(2,4-dimethoxyphenyl) ditelluride | 158667-06-2

中文名称
——
中文别名
——
英文名称
bis(2,4-dimethoxyphenyl) ditelluride
英文别名
bis(2,4-dimethoxyphenyl)ditelluride;bis-(2,4-dimethoxy-phenyl)-ditelluride;Bis-(2,4-dimethoxy-phenyl)-ditellurid;1-[(2,4-Dimethoxyphenyl)ditellanyl]-2,4-dimethoxybenzene
bis(2,4-dimethoxyphenyl) ditelluride化学式
CAS
158667-06-2
化学式
C16H18O4Te2
mdl
——
分子量
529.517
InChiKey
UBQIIUMHOTXLOU-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):
    1.0
  • 重原子数:
    22
  • 可旋转键数:
    7
  • 环数:
    2.0
  • 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

反应信息

  • 作为反应物:
    描述:
    bis(2,4-dimethoxyphenyl) ditelluride 在 sodium tetrahydroborate 作用下, 以 为溶剂, 反应 0.75h, 生成 3-<<(2,4-dimethoxyphenyl)telluro>methyl>chromanone
    参考文献:
    名称:
    Photoinduced Free Radical Chemistry of the Acyl Tellurides: Generation, Inter- and Intramolecular Trapping, and ESR Spectroscopic Identification of Acyl Radicals
    摘要:
    Acyl tellurides are prepared in good to excellent yield by the reaction of sodium aryl tellurides with acyl chlorides, or mixed anhydrides, and are found to be moderately air-stable substances. In contrast to previous literature reports, acyl tellurides of aryl and vinyl carboxylic acids are found to be excellent sources of acyl radicals on photolysis with a simple white light source. The acyl radicals so generated may be trapped intermolecularly by dichalcogenides, or by TEMPO in excellent yield. Trapping by N-tert-butyl-alpha-phenyl nitrone produces a stable nitroxide radical which has been characterized by ESR spectroscopy. The very efficient trapping of acyl radicals by acyl tellurides themselves is demonstrated by a crossover experiment. Acyl tellurides are shown to participate in very efficient radical cyclization reactions onto alkenes with the formation of five-, six-, and eight-membered rings. The immediate products of the cyclizations onto alkenes are alpha-[(aryltelluro)methyl] ketones and the chemistry of these relatively unstable species is briefly described. Treatment with hydrogen peroxide affords alpha-methylene ketones in high yield. When elimination of the aryl telluro group is not possible the alpha-[(aryltelluro)methyl] ketones are stable species that may subsequently be employed in further radical chain reactions, for example with tributyltin hydride and methyl acrylate. Cyclization onto alkynes yields alpha-[(aryltelluro)methylene] ketones which are stable species and which take part in substitution reactions with higher order cuprates or with diphenyl diselenide.
    DOI:
    10.1021/ja00099a011
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 potassium disulphite 、 作用下, 生成 bis(2,4-dimethoxyphenyl) ditelluride
    参考文献:
    名称:
    Morgan; Drew, Journal of the Chemical Society, 1925, vol. 127, p. 2314
    摘要:
    DOI:
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文献信息

  • The chemistry of acyl tellurides: generation and trapping of acyl radicals, including aryltellurium group transfer
    作者:Chen Chen、David Crich、Aristotle Papadatos
    DOI:10.1021/ja00047a066
    日期:1992.10
  • Buzilova,S.R. et al., Journal of general chemistry of the USSR, 1977, vol. 47, p. 1828 - 1831
    作者:Buzilova,S.R. et al.
    DOI:——
    日期:——
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