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2-((l4-boraneyl)(methyl)-l5-phosphaneyl)propan-2-ol | 190836-01-2

中文名称
——
中文别名
——
英文名称
2-((l4-boraneyl)(methyl)-l5-phosphaneyl)propan-2-ol
英文别名
——
2-((l4-boraneyl)(methyl)-l5-phosphaneyl)propan-2-ol化学式
CAS
190836-01-2
化学式
C4H14BOP
mdl
——
分子量
119.939
InChiKey
GXDYVYTVEPPQIX-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为产物:
    描述:
    methylphosphine borane 、 丙酮 为溶剂, 以30%的产率得到2-((l4-boraneyl)(methyl)-l5-phosphaneyl)propan-2-ol
    参考文献:
    名称:
    PH bond activation of primary phosphine-boranes: Access to α-hydroxy and α,α′-dihydroxyphosphine-borane adducts by uncatalyzed hydrophosphination of carbonyl derivatives
    摘要:
    Primary P-phenyl and P-methyl phosphine-boranes 1 and 2 are prepared by complexation of the free phosphines with BH3 . SMe2. They are stable and can be purified by distillation. Under basic conditions, they lead selectively to secondary alkylphosphine-boranes and under neutral conditions to the corresponding mono- and bis-hydroxyphosphine-boranes 5 and 6. All these new compounds are purified by chromatography on silica gel. A competitive hydroboration induced by the decomplexation of BH3 is observed as a minor process. Conditions for the decomplexation of phosphine-borane adducts are presented.
    DOI:
    10.1016/s0022-328x(96)06640-5
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