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3-hydroxy-5-phenyl-2,3-dihydrofuran-3,4-dicarboxylic acid diethyl ester | 1048023-95-5

中文名称
——
中文别名
——
英文名称
3-hydroxy-5-phenyl-2,3-dihydrofuran-3,4-dicarboxylic acid diethyl ester
英文别名
diethyl 3-hydroxy-5-phenyl-2H-furan-3,4-dicarboxylate
3-hydroxy-5-phenyl-2,3-dihydrofuran-3,4-dicarboxylic acid diethyl ester化学式
CAS
1048023-95-5
化学式
C16H18O6
mdl
——
分子量
306.315
InChiKey
BFCBKZRDVBCBDB-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):
    2.1
  • 重原子数:
    22
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    82.1
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    3-溴丙酮酸乙酯苯甲酰乙酸乙酯1-butyl-3-methylimidazolium hydroxide 作用下, 反应 4.0h, 以60%的产率得到3-hydroxy-5-phenyl-2,3-dihydrofuran-3,4-dicarboxylic acid diethyl ester
    参考文献:
    名称:
    Ionic liquid promoted interrupted Feist–Benary reaction with high diastereoselectivity
    摘要:
    A basic ionic liquid, 1-butyl-3-methylimidazolium hydroxide promotes the interrupted Feist-Eenary reaction at room temperature under organic solvent-ftee conditions to produce a variety of substituted hydFOxydihydrofurans. The hydroxydihydrofurans are converted to furans (Feist-Benary products) using the ionic liquid, 1-methyl-3-pentylimidazolium bromide at 70-75 degrees C. The reactions are very clean, high yielding and highly stereoselective. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.05.083
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文献信息

  • Ionic liquid promoted interrupted Feist–Benary reaction with high diastereoselectivity
    作者:Brindaban C. Ranu、Laksmikanta Adak、Subhash Banerjee
    DOI:10.1016/j.tetlet.2008.05.083
    日期:2008.7
    A basic ionic liquid, 1-butyl-3-methylimidazolium hydroxide promotes the interrupted Feist-Eenary reaction at room temperature under organic solvent-ftee conditions to produce a variety of substituted hydFOxydihydrofurans. The hydroxydihydrofurans are converted to furans (Feist-Benary products) using the ionic liquid, 1-methyl-3-pentylimidazolium bromide at 70-75 degrees C. The reactions are very clean, high yielding and highly stereoselective. (c) 2008 Elsevier Ltd. All rights reserved.
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