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ethyl 3-benzhydrylidene-4,4-dicyano-5-[(E)-2-phenylethenyl]cyclopentene-1-carboxylate | 1119249-71-6

中文名称
——
中文别名
——
英文名称
ethyl 3-benzhydrylidene-4,4-dicyano-5-[(E)-2-phenylethenyl]cyclopentene-1-carboxylate
英文别名
——
ethyl 3-benzhydrylidene-4,4-dicyano-5-[(E)-2-phenylethenyl]cyclopentene-1-carboxylate化学式
CAS
1119249-71-6
化学式
C31H24N2O2
mdl
——
分子量
456.544
InChiKey
HFQRPUOAMKTSBX-VHEBQXMUSA-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:
    694.0±55.0 °C(predicted)
  • 密度:
    1.22±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.4
  • 重原子数:
    35
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    73.9
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    ethyl 5,5-diphenylpenta-2,3,4-trienoate(E)-2-(3-phenylallylidene)malononitrile三丁基膦 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 以86%的产率得到ethyl 3-benzhydrylidene-4,4-dicyano-5-[(E)-2-phenylethenyl]cyclopentene-1-carboxylate
    参考文献:
    名称:
    Phosphine-Mediated [3+2] Cycloaddition Reactions of Ethyl 5,5-Diarylpenta-2,3,4-trienoates with Arylmethylidenemalononitriles and N-Tosylimines
    摘要:
    Ethyl 5,5-diaryipenta-2,3,4-trienoates were synthesized and utilized in the phosphine-mediated [3+2] cycloaddition reactions with arylmethylidenemalononitriles and N-tosylimines in the presence of tributylphosphine. These reactions provide an easy access to a variety of novel polysubstituted cyclopentenes or pyrrolidines in good to excellent yields under mild conditions.
    DOI:
    10.1021/jo802489t
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文献信息

  • Phosphine-Mediated [3+2] Cycloaddition Reactions of Ethyl 5,5-Diarylpenta-2,3,4-trienoates with Arylmethylidenemalononitriles and <i>N</i>-Tosylimines
    作者:Xiao-Yang Guan、Min Shi
    DOI:10.1021/jo802489t
    日期:2009.3.6
    Ethyl 5,5-diaryipenta-2,3,4-trienoates were synthesized and utilized in the phosphine-mediated [3+2] cycloaddition reactions with arylmethylidenemalononitriles and N-tosylimines in the presence of tributylphosphine. These reactions provide an easy access to a variety of novel polysubstituted cyclopentenes or pyrrolidines in good to excellent yields under mild conditions.
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