摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

bis(β,β,β-trichloro-α-hydroxyethyl)(o-hydroxyphenyl)phosphine | 133859-81-1

中文名称
——
中文别名
——
英文名称
bis(β,β,β-trichloro-α-hydroxyethyl)(o-hydroxyphenyl)phosphine
英文别名
Bis(beta,beta,beta-trichloro-alpha-hydroxyethyl)(o-hydroxyphenyl)phosphine;2-bis(2,2,2-trichloro-1-hydroxyethyl)phosphanylphenol
bis(β,β,β-trichloro-α-hydroxyethyl)(o-hydroxyphenyl)phosphine化学式
CAS
133859-81-1
化学式
C10H9Cl6O3P
mdl
——
分子量
420.871
InChiKey
CYFASECMACSYQV-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):
    3.8
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    60.7
  • 氢给体数:
    3
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    bis(β,β,β-trichloro-α-hydroxyethyl)(o-hydroxyphenyl)phosphine苯硼酸 为溶剂, 以43%的产率得到(2-phenyl-4,6-bis(trichloromethyl)-5-o-hydroxyphenyl-1,3,2,5-dioxabora)phosphorinane
    参考文献:
    名称:
    Borylation of o-Hydroxyphenyl phosphorus derivatives
    摘要:
    The reactions of isobutyl diphenylborate with O,O-diethyl o-hydroxyphenylphosphonate and o-hydroxyphenylphosphine gave 5,6-benzo-2-phenyl-4-ethoxy-4-oxo-1,3,2,4-dioxaboraphosphorinane and o-diphenylboryloxyphenylphosphine, respectively. The borylation only at the alpha-hydroxyalkyl fragments of bis(beta,beta,beta-trichloro-alpha-hydroxyethyl)(o-hydroxyphenyl)phosphine and the conversion of the o-boryloxyphenyl phosphorus derivative to an alpha-boryloxyalkyl derivative upon the action of chloral indicates the greater stability of compounds with the P-C-O-B fragment than that for compounds with the P-C-C-O-B fragment.
    DOI:
    10.1007/bf00965441
  • 作为产物:
    描述:
    邻羟基苯基膦三氯乙醛乙醚 为溶剂, 反应 1.0h, 以95%的产率得到bis(β,β,β-trichloro-α-hydroxyethyl)(o-hydroxyphenyl)phosphine
    参考文献:
    名称:
    Borylation of o-Hydroxyphenyl phosphorus derivatives
    摘要:
    The reactions of isobutyl diphenylborate with O,O-diethyl o-hydroxyphenylphosphonate and o-hydroxyphenylphosphine gave 5,6-benzo-2-phenyl-4-ethoxy-4-oxo-1,3,2,4-dioxaboraphosphorinane and o-diphenylboryloxyphenylphosphine, respectively. The borylation only at the alpha-hydroxyalkyl fragments of bis(beta,beta,beta-trichloro-alpha-hydroxyethyl)(o-hydroxyphenyl)phosphine and the conversion of the o-boryloxyphenyl phosphorus derivative to an alpha-boryloxyalkyl derivative upon the action of chloral indicates the greater stability of compounds with the P-C-O-B fragment than that for compounds with the P-C-C-O-B fragment.
    DOI:
    10.1007/bf00965441
点击查看最新优质反应信息

文献信息

  • BALUEVA, I. S.;NIKONOV, G. N.;VULFSON, S. G.;SARVAROVA, N. N.;ARBUZOV, B.+, IZV. AN CCCP. CEP. XIM.,(1991) N, S. 477-482
    作者:BALUEVA, I. S.、NIKONOV, G. N.、VULFSON, S. G.、SARVAROVA, N. N.、ARBUZOV, B.+
    DOI:——
    日期:——
查看更多