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tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)methanol

中文名称
——
中文别名
——
英文名称
tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)methanol
英文别名
1,1,1,2,2,3,3,4,4,5,5,6,6,12,12,13,13,14,14,15,15,16,16,17,17,17-Hexacosafluoro-9-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)heptadecan-9-ol
tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)methanol化学式
CAS
——
化学式
C25H13F39O
mdl
——
分子量
1070.32
InChiKey
JIPYTADEEBFFJG-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):
    15
  • 重原子数:
    65
  • 可旋转键数:
    21
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    40

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    去甲麻黄碱甲苯tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)methanol三氟甲磺酸N-溴代丁二酰亚胺(NBS)偶氮二异丁腈potassium carbonate 作用下, 以 四氯化碳四氢呋喃 为溶剂, 反应 40.0h, 以223 mg的产率得到(1R,2S)-N,N-bis[4-tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)methyl]benzylnorephedrine
    参考文献:
    名称:
    Enantioselective addition of diethylzinc to aldehydes catalyzed by fluorous β-aminoalcohols
    摘要:
    A fluorous aminoalcohol prepared from ephedrine has been used as a catalyst for the enantioselective addition of diethylzinc to aldehydes to afford the corresponding alcohols in up to 84% ee. The fluorous amino alcohol was easily recovered by a simple filtration through a fluorous reverse phase silica gel and was reusable without purification. (C) 2001 Elsevier Science Ltd. AU rights reserved.
    DOI:
    10.1016/s0040-4020(01)00483-5
  • 作为产物:
    描述:
    1-碘-1H,1H,2H,2H-全氟辛烷碳酸二甲酯magnesium 作用下, 以 乙醚 为溶剂, 以40%的产率得到tris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)methanol
    参考文献:
    名称:
    Enantioselective addition of diethylzinc to aldehydes catalyzed by fluorous β-aminoalcohols
    摘要:
    A fluorous aminoalcohol prepared from ephedrine has been used as a catalyst for the enantioselective addition of diethylzinc to aldehydes to afford the corresponding alcohols in up to 84% ee. The fluorous amino alcohol was easily recovered by a simple filtration through a fluorous reverse phase silica gel and was reusable without purification. (C) 2001 Elsevier Science Ltd. AU rights reserved.
    DOI:
    10.1016/s0040-4020(01)00483-5
  • 作为试剂:
    描述:
    丙烯酰碘methyl(1-methyl-1-phenylethyl)ketenetris(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)methanol 六甲基磷酰三胺 、 samarium diiodide 、 DHPEX C2-symmetric chiral diol 作用下, 以95%的产率得到(R)-5,6-dimethyl-6-phenyl-1-hepten-4-one
    参考文献:
    名称:
    氟双相体系中氟的手性和非手性质子源对烯醇mar的催化对映选择性质子化。
    摘要:
    由ropid添加氟的非手性醇(RFH的催化反应获得接近最大值的对映选择性3为DHPEX在RFH:COH)加入到反应混合物3 COH/ THF固液两相体系和用于氟THF / FC-72液-液双相系统中的手性醇。
    DOI:
    10.1016/s0040-4039(98)01900-5
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文献信息

  • Enantioselective addition of diethylzinc to aldehydes catalyzed by fluorous β-aminoalcohols
    作者:Yutaka Nakamura、Seiji Takeuchi、Kazuo Okumura、Yoshiaki Ohgo
    DOI:10.1016/s0040-4020(01)00483-5
    日期:2001.6
    A fluorous aminoalcohol prepared from ephedrine has been used as a catalyst for the enantioselective addition of diethylzinc to aldehydes to afford the corresponding alcohols in up to 84% ee. The fluorous amino alcohol was easily recovered by a simple filtration through a fluorous reverse phase silica gel and was reusable without purification. (C) 2001 Elsevier Science Ltd. AU rights reserved.
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