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1,1,1-Trifluoro-5-trimethylsilanyl-pent-4-yn-2-ol | 212758-87-7

中文名称
——
中文别名
——
英文名称
1,1,1-Trifluoro-5-trimethylsilanyl-pent-4-yn-2-ol
英文别名
1,1,1-Trifluoro-5-(trimethylsilyl)pent-4-yn-2-ol;1,1,1-trifluoro-5-trimethylsilylpent-4-yn-2-ol
1,1,1-Trifluoro-5-trimethylsilanyl-pent-4-yn-2-ol化学式
CAS
212758-87-7
化学式
C8H13F3OSi
mdl
——
分子量
210.271
InChiKey
MGSIJUFDXHZURG-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):
    2.18
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    1,1,1-Trifluoro-5-trimethylsilanyl-pent-4-yn-2-ol二异丁基氢化铝 作用下, 以 乙醚正己烷 为溶剂, 反应 24.0h, 以61%的产率得到(Z)-1,1,1-Trifluoro-5-(trimethylsilyl)-4-pentene-2-ol
    参考文献:
    名称:
    Rapid access to CF3-containing heterocycles
    摘要:
    The silyl-Prins and aza-silyl-Prins reactions have been employed for the preparation of 6-CF3-substituted dihydropyrans and 6-CF3-substituted tetrahydropyridines. The product heterocycles have been further elaborated to a number of products, including CF3-substituted pipecolates and hydroxylated pyrans and piperidines. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.11.178
  • 作为产物:
    描述:
    1,1,1-三氟-2,3-环氧丙烷三甲基乙炔基硅正丁基锂氯化二乙基铝 作用下, 以 正己烷 为溶剂, 以82%的产率得到1,1,1-Trifluoro-5-trimethylsilanyl-pent-4-yn-2-ol
    参考文献:
    名称:
    Rapid access to CF3-containing heterocycles
    摘要:
    The silyl-Prins and aza-silyl-Prins reactions have been employed for the preparation of 6-CF3-substituted dihydropyrans and 6-CF3-substituted tetrahydropyridines. The product heterocycles have been further elaborated to a number of products, including CF3-substituted pipecolates and hydroxylated pyrans and piperidines. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.11.178
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文献信息

  • Facile and Selective Alkylation of 3,3,3-Trifluoropropene Oxide (TFPO) with Organoaluminum Reagents via Pentacoordinate Trialkylaluminum Complexes
    作者:Takashi Ooi、Mayumi Furuya、Keiji Maruoka
    DOI:10.1246/cl.1998.817
    日期:1998.8
    A new organoaluminum-promoted selective alkylation of 3,3,3-trifluoropropene oxide (TFPO) with several nucleophiles has been developed which involves the chelation-activated addition to fluoro epoxides via pentacoordinate trialkylaluminum complexes.
    已经开发了一种新的有机铝促进的 3,3,3-三环氧丙烷 (TFPO) 与几种亲核试剂的选择性烷基化,其中涉及通过五配位三烷基铝配合物螯合活化加成到环氧化物中。
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