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Ethyl (+/-)-3-hydroxy-2,2-dimethyl-3-phenylhexanoate

中文名称
——
中文别名
——
英文名称
Ethyl (+/-)-3-hydroxy-2,2-dimethyl-3-phenylhexanoate
英文别名
Ethyl 3-hydroxy-2,2-dimethyl-3-phenylhexanoate
Ethyl (+/-)-3-hydroxy-2,2-dimethyl-3-phenylhexanoate化学式
CAS
——
化学式
C16H24O3
mdl
MFCD17339080
分子量
264.365
InChiKey
DZZPNUSKHDUUJY-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):
    3.3
  • 重原子数:
    19
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.562
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis of .alpha.,.alpha.,.beta.,.beta.-Tetrasubstituted .beta.-Lactones from Ketones, Ethyl .alpha.-Bromoisobutyrate, and Indium or Zinc. Factors Influencing the .beta.-Lactone Formation in the Electrochemical and the Classical Procedure of the Reformatsky Reaction
    摘要:
    An efficient synthesis of alpha,alpha,beta,beta-tetrasubstituted beta-lactones is achieved by an electrochemically supported Reformatsky reaction of aliphatic and aromatic ketones with ethyl alpha-bromoisobutyrate at a sacrificial indium anode. Under these conditions, in most cases the expected beta-hydroxy esters are formed only in negligible amounts or not at all. beta-Lactones are also obtained with a sacrificial zinc anode or even with indium or zinc powder. The substitution pattern of the reactants, the polarity of the solvent, and the applied metal are recognized as factors influencing the extent of the beta-lactone formation.
    DOI:
    10.1021/jo00090a038
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文献信息

  • Synthesis of .alpha.,.alpha.,.beta.,.beta.-Tetrasubstituted .beta.-Lactones from Ketones, Ethyl .alpha.-Bromoisobutyrate, and Indium or Zinc. Factors Influencing the .beta.-Lactone Formation in the Electrochemical and the Classical Procedure of the Reformatsky Reaction
    作者:Hans Schick、Ralf Ludwig、Karl-Heinz Schwarz、Katharina Kleiner、Annamarie Kunath
    DOI:10.1021/jo00090a038
    日期:1994.6
    An efficient synthesis of alpha,alpha,beta,beta-tetrasubstituted beta-lactones is achieved by an electrochemically supported Reformatsky reaction of aliphatic and aromatic ketones with ethyl alpha-bromoisobutyrate at a sacrificial indium anode. Under these conditions, in most cases the expected beta-hydroxy esters are formed only in negligible amounts or not at all. beta-Lactones are also obtained with a sacrificial zinc anode or even with indium or zinc powder. The substitution pattern of the reactants, the polarity of the solvent, and the applied metal are recognized as factors influencing the extent of the beta-lactone formation.
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