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ethyl 3-fluoro-2-(phenylselenyl)butanoate | 1131125-58-0

中文名称
——
中文别名
——
英文名称
ethyl 3-fluoro-2-(phenylselenyl)butanoate
英文别名
Ethyl 3-fluoro-2-phenylselanylbutanoate
ethyl 3-fluoro-2-(phenylselenyl)butanoate化学式
CAS
1131125-58-0
化学式
C12H15FO2Se
mdl
——
分子量
289.208
InChiKey
WPWMMNAHIMZOPA-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:
    336.2±42.0 °C(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.73
  • 重原子数:
    16
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    二苯基二硒醚反式-2-丁烯酸乙酯 在 triethylamine pentahydrogen fluoride salt 作用下, 以 硝基甲烷 为溶剂, 以71%的产率得到ethyl 3-fluoro-2-(phenylselenyl)butanoate
    参考文献:
    名称:
    Electrochemical fluoro-selenenylation of electron-deficient olefins
    摘要:
    Electrochemical fluoro-selenenylation of electron-deficient olefins like a,p-unsaturated ester, carboxylic acid, amide, and phosphonate was successfully carried out by the anodic oxidation of diphenyl diselenide in the presence of olefins in Et3N center dot 5HF/CH3NO2. The anodically generated benzeneselenenyl fluoride [PhSeF] equivalent was stable in the electrolytic solution, which resulted in the efficient fluoro-selenenylation. The fluoro-selenenylation products were shown to be potential useful fluoro-building blocks. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.12.068
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文献信息

  • Electrochemical fluoro-selenenylation of electron-deficient olefins
    作者:Hirokatsu Nagura、Shinsuke Inagi、Toshio Fuchigami
    DOI:10.1016/j.tet.2008.12.068
    日期:2009.2
    Electrochemical fluoro-selenenylation of electron-deficient olefins like a,p-unsaturated ester, carboxylic acid, amide, and phosphonate was successfully carried out by the anodic oxidation of diphenyl diselenide in the presence of olefins in Et3N center dot 5HF/CH3NO2. The anodically generated benzeneselenenyl fluoride [PhSeF] equivalent was stable in the electrolytic solution, which resulted in the efficient fluoro-selenenylation. The fluoro-selenenylation products were shown to be potential useful fluoro-building blocks. (C) 2008 Elsevier Ltd. All rights reserved.
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