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2-bromo-3-(4-bromophenoxy)-1-propanol | 145733-78-4

中文名称
——
中文别名
——
英文名称
2-bromo-3-(4-bromophenoxy)-1-propanol
英文别名
2-Bromo-3-(4-bromophenoxy)propan-1-ol
2-bromo-3-(4-bromophenoxy)-1-propanol化学式
CAS
145733-78-4
化学式
C9H10Br2O2
mdl
——
分子量
309.985
InChiKey
AJGHAKFCIKXSMW-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):
    2.7
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    苯基缩水甘油醚 作用下, 以 乙腈 为溶剂, 以44%的产率得到2-bromo-3-(4-bromophenoxy)-1-propanol
    参考文献:
    名称:
    Conversion of epoxides into halohydrins with elemental halogen catalyzed by thiourea
    摘要:
    A highly regioselective method for the synthesis of beta-iodohydrins and beta-bromohydrins by the direct ring opening of epoxides with elemental halogen in the presence of thiourea is described. This method occurs under neutral and mild conditions with high yields in various solvents even when sensitive functional groups are present. (C) 2003 Published by Elsevier Ltd.
    DOI:
    10.1016/j.tet.2003.09.033
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文献信息

  • Halogenation reactions of epoxides
    作者:Monica I. Konaklieva、Michele L. Dahl、Edward Turos
    DOI:10.1016/s0040-4039(00)60844-4
    日期:1992.11
    The halogenation of aryl and alkyl epoxides using elemental bromine or iodine has been studied.
  • US4209639A
    申请人:——
    公开号:US4209639A
    公开(公告)日:1980-06-24
  • Conversion of epoxides into halohydrins with elemental halogen catalyzed by thiourea
    作者:Hashem Sharghi、Mohammad Mehdi Eskandari
    DOI:10.1016/j.tet.2003.09.033
    日期:2003.10
    A highly regioselective method for the synthesis of beta-iodohydrins and beta-bromohydrins by the direct ring opening of epoxides with elemental halogen in the presence of thiourea is described. This method occurs under neutral and mild conditions with high yields in various solvents even when sensitive functional groups are present. (C) 2003 Published by Elsevier Ltd.
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