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(E)-1,1,1,2,4,4,4-heptafluoro-2-butene | 19804-68-3

中文名称
——
中文别名
——
英文名称
(E)-1,1,1,2,4,4,4-heptafluoro-2-butene
英文别名
(E)-1,1,1,3,4,4,4-Heptafluoro-2-butene;(E)-1,1,1,2,4,4,4-heptafluorobut-2-ene
(E)-1,1,1,2,4,4,4-heptafluoro-2-butene化学式
CAS
19804-68-3
化学式
C4HF7
mdl
——
分子量
182.041
InChiKey
YIFLMZOLKQBEBO-OWOJBTEDSA-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):
    2.6
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    7

SDS

SDS:98362bedc3d3fc97acb6100c2b410831
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反应信息

  • 作为产物:
    描述:
    1,1,1,2,4,4,4-Heptafluoro-3-iodobut-2-ene 在 作用下, 生成 (E)-1,1,1,2,4,4,4-heptafluoro-2-butene(Z)-1,1,1,2,4,4,4-heptafluoro-but-2-ene六氟-2-丁炔
    参考文献:
    名称:
    Preparation of the E- and Z-heptafluorobutenyl-2-zinc reagent by zinc-induced dehalogenation/metallation of 2,2-dibromo-octafluorobutane
    摘要:
    The AlCl3-catalyzed isomerization of CF3CFBrCFBrCF3 afforded CF3CF2CBr2CF3, which upon treatment with 2 equiv. zinc in DMF underwent dehalogenation/metallation to afford a 1:1 mixture of E- and Z-CF3CF=C(ZnX)CF3 in 96% F-19 NMR yield. The zinc reagent exhibited poor thermal stability in DMF and completely decomposed by a beta-elimination route in 24 h at 60-degrees-C. However, the zinc reagent prepared from E- and Z-CF3CF=CICF3 in triglyme showed enhanced thermal stability and gave E- and Z-p-NO2C6H4C(CF3)=CFCF3 in a palladium-catalyzed coupling reaction with p-NO2C6H4I.
    DOI:
    10.1016/0022-1139(93)02905-t
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文献信息

  • Preparation of the E- and Z-heptafluorobutenyl-2-zinc reagent by zinc-induced dehalogenation/metallation of 2,2-dibromo-octafluorobutane
    作者:Peter A. Morken、Robert F. Campbell、Donald J. Burton
    DOI:10.1016/0022-1139(93)02905-t
    日期:1994.1
    The AlCl3-catalyzed isomerization of CF3CFBrCFBrCF3 afforded CF3CF2CBr2CF3, which upon treatment with 2 equiv. zinc in DMF underwent dehalogenation/metallation to afford a 1:1 mixture of E- and Z-CF3CF=C(ZnX)CF3 in 96% F-19 NMR yield. The zinc reagent exhibited poor thermal stability in DMF and completely decomposed by a beta-elimination route in 24 h at 60-degrees-C. However, the zinc reagent prepared from E- and Z-CF3CF=CICF3 in triglyme showed enhanced thermal stability and gave E- and Z-p-NO2C6H4C(CF3)=CFCF3 in a palladium-catalyzed coupling reaction with p-NO2C6H4I.
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