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1-butylpentyl trifluoromethanesulfonate

中文名称
——
中文别名
——
英文名称
1-butylpentyl trifluoromethanesulfonate
英文别名
Nonan-5-yl trifluoromethanesulfonate
1-butylpentyl trifluoromethanesulfonate化学式
CAS
——
化学式
C10H19F3O3S
mdl
——
分子量
276.32
InChiKey
BFQHOACGWRKDKD-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):
    4.5
  • 重原子数:
    17
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    51.8
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    1-butylpentyl trifluoromethanesulfonate4,4'-二叔丁基苯并lithium 作用下, 以 四氢呋喃 为溶剂, 反应 4.0h, 以68%的产率得到正壬烷
    参考文献:
    名称:
    Reduction of alkyl and vinyl sulfonates using the CuCl2·2H2O–Li–DTBB(cat.) system
    摘要:
    The reduction of a series of alkyl mesylates, dimesylates and triflates to the corresponding hydrocarbons was efficiently performed using a reducing system composed of CuCl2 center dot 2H(2)O, an excess of lithium sand and a catalytic amount (5 mol%) of 4,4'-di-tertbutylbiphenyl (DTBB), in tetrahydrofuran at room temperature. The process was also applied to enol and dienol triflates affording alkenes and dienes, respectively. The use of the deuterated copper salt CuCl2 center dot 2D(2)O allowed the simple preparation of the corresponding deuterated products. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2005.01.078
  • 作为产物:
    描述:
    5-壬醇三氟甲磺酸酐吡啶 作用下, 反应 25.0h, 生成 1-butylpentyl trifluoromethanesulfonate
    参考文献:
    名称:
    Reduction of alkyl and vinyl sulfonates using the CuCl2·2H2O–Li–DTBB(cat.) system
    摘要:
    The reduction of a series of alkyl mesylates, dimesylates and triflates to the corresponding hydrocarbons was efficiently performed using a reducing system composed of CuCl2 center dot 2H(2)O, an excess of lithium sand and a catalytic amount (5 mol%) of 4,4'-di-tertbutylbiphenyl (DTBB), in tetrahydrofuran at room temperature. The process was also applied to enol and dienol triflates affording alkenes and dienes, respectively. The use of the deuterated copper salt CuCl2 center dot 2D(2)O allowed the simple preparation of the corresponding deuterated products. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2005.01.078
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文献信息

  • Reduction of alkyl and vinyl sulfonates using the CuCl2·2H2O–Li–DTBB(cat.) system
    作者:Gabriel Radivoy、Francisco Alonso、Yanina Moglie、Cristian Vitale、Miguel Yus
    DOI:10.1016/j.tet.2005.01.078
    日期:2005.4
    The reduction of a series of alkyl mesylates, dimesylates and triflates to the corresponding hydrocarbons was efficiently performed using a reducing system composed of CuCl2 center dot 2H(2)O, an excess of lithium sand and a catalytic amount (5 mol%) of 4,4'-di-tertbutylbiphenyl (DTBB), in tetrahydrofuran at room temperature. The process was also applied to enol and dienol triflates affording alkenes and dienes, respectively. The use of the deuterated copper salt CuCl2 center dot 2D(2)O allowed the simple preparation of the corresponding deuterated products. (c) 2005 Elsevier Ltd. All rights reserved.
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