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Chloromethyl-dimethyl-(thiophen-2-ylmethyl)silane | 187337-31-1

中文名称
——
中文别名
——
英文名称
Chloromethyl-dimethyl-(thiophen-2-ylmethyl)silane
英文别名
——
Chloromethyl-dimethyl-(thiophen-2-ylmethyl)silane化学式
CAS
187337-31-1
化学式
C8H13ClSSi
mdl
——
分子量
204.796
InChiKey
LTXPADYNHSJRMI-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):
    3.32
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    28.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    苯甲醛Chloromethyl-dimethyl-(thiophen-2-ylmethyl)silanemagnesium 作用下, 生成 2-[Dimethyl(thiophen-2-ylmethyl)silyl]-1-phenylethanol
    参考文献:
    名称:
    Synthesis of Thiophene Derivatives Bearing a Silicon Atom
    摘要:
    Synthesis of thiophene derivatives containing a silicon atom is described. Silylation of 2-thienylmethyl chloride (12) with trichlorovinylsilane or chloro(chloromethyl)dimethylsilane was accomplished by addition of 12 to a mixture of Mg and the former reagent in THF or by addition of a mixture of 12 and the latter reagent to a mixture of Mg in THF to give dichloro(2-thienylmethyl)vinylsilane (13) or chloromethyl(dimethyl)(2-thienylmethyl) (18). The Grignard reagent (19) of 18 reacted with carbon dioxide, dimethyl carbonate or benzaldehyde to produce dimethyl(2-thienylmethyl)silylacetic acid (20), methyl dimethyl(2-thienylmethyl)silylacetate (21) or 2'-[dimethyl(2-thienylmethyl)silyl]-1'-phenylethanol (22).
    DOI:
    10.3987/com-96-s51
  • 作为产物:
    描述:
    2-噻吩甲醇吡啶氯化亚砜magnesium 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 2.17h, 生成 Chloromethyl-dimethyl-(thiophen-2-ylmethyl)silane
    参考文献:
    名称:
    Synthesis of Thiophene Derivatives Bearing a Silicon Atom
    摘要:
    Synthesis of thiophene derivatives containing a silicon atom is described. Silylation of 2-thienylmethyl chloride (12) with trichlorovinylsilane or chloro(chloromethyl)dimethylsilane was accomplished by addition of 12 to a mixture of Mg and the former reagent in THF or by addition of a mixture of 12 and the latter reagent to a mixture of Mg in THF to give dichloro(2-thienylmethyl)vinylsilane (13) or chloromethyl(dimethyl)(2-thienylmethyl) (18). The Grignard reagent (19) of 18 reacted with carbon dioxide, dimethyl carbonate or benzaldehyde to produce dimethyl(2-thienylmethyl)silylacetic acid (20), methyl dimethyl(2-thienylmethyl)silylacetate (21) or 2'-[dimethyl(2-thienylmethyl)silyl]-1'-phenylethanol (22).
    DOI:
    10.3987/com-96-s51
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