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triethylammonium 2,2,4,5,6-pentaphenyl-1,3,2,5-dioxaborataphosphorinane

中文名称
——
中文别名
——
英文名称
triethylammonium 2,2,4,5,6-pentaphenyl-1,3,2,5-dioxaborataphosphorinane
英文别名
2,2,4,5,6-Pentakis-phenyl-1,3-dioxa-5-phospha-2-boranuidacyclohexane;triethylazanium
triethylammonium 2,2,4,5,6-pentaphenyl-1,3,2,5-dioxaborataphosphorinane化学式
CAS
——
化学式
C6H16N*C32H27BO2P
mdl
——
分子量
587.55
InChiKey
PRXLAVBTRYJJCF-UHFFFAOYSA-O
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):
    6.43
  • 重原子数:
    43
  • 可旋转键数:
    8
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    22.9
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1,3-di-tert-octyl-5-methyl-5-phenyl-1,3,5-diazaphosphoniarinane iodide 、 triethylammonium 2,2,4,5,6-pentaphenyl-1,3,2,5-dioxaborataphosphorinane乙腈 为溶剂, 以18%的产率得到5-methyl-2,2,4,5,6-pentaphenyl-1,3,2,5-dioxaborataphosphoniarinane
    参考文献:
    名称:
    Synthesis and properties of triethylammonium 2,2,5-triphenyl-1,3,2,5-dioxaborataphosphorinane
    摘要:
    The reaction of bis(hydroxymethyl)phenylphosphine with isobutyl diphenylborate in the presence of triethylamine leads to the formation of triethylammonium 2,2,5-triphenyl-1,3,2,5-dioxaborataphosphorinane (1). The reaction of compound 1 with electrophilic reagents (O, S, Se, CH2O, RHal) leads to quaternization of the phosphorus atom, giving the corresponding phosphine oxides, sulfides, and selenides and PB-containing betaines. In the reactions of compound 1 with amines aminoniethylphosphines of the diazaphosphorinane and diazadiphosphacyclooctane series are formed. Ammonium 1,3,2,5-dioxaborataphosphorinanes dissociate in solutions and enter into ion exchange with phosphonium iodides, leading to phosphonium 1,3,2,5-dioxaborataphosphorinanes. The latter. in the case of the aminomethylphosphonium cation, undergo intramolecular rearrangement with the formation of PB-containing betaines and aminomethylphosphines.
    DOI:
    10.1007/bf00866594
  • 作为产物:
    描述:
    bis(α-hydroxybenzyl)phenylphosphine2-甲基丙氧基(二苯基)硼烷三乙胺 作用下, 以 三乙胺 为溶剂, 以94%的产率得到triethylammonium 2,2,4,5,6-pentaphenyl-1,3,2,5-dioxaborataphosphorinane
    参考文献:
    名称:
    Synthesis of ammonium 1,3,2,5-dioxaborataphosphorinanes
    摘要:
    DOI:
    10.1007/bf00954832
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文献信息

  • Synthesis and properties of triethylammonium 2,2,5-triphenyl-1,3,2,5-dioxaborataphosphorinane
    作者:G. N. Nikonov、A. A. Karasik、B. A. Arbuzov
    DOI:10.1007/bf00866594
    日期:1992.6
    The reaction of bis(hydroxymethyl)phenylphosphine with isobutyl diphenylborate in the presence of triethylamine leads to the formation of triethylammonium 2,2,5-triphenyl-1,3,2,5-dioxaborataphosphorinane (1). The reaction of compound 1 with electrophilic reagents (O, S, Se, CH2O, RHal) leads to quaternization of the phosphorus atom, giving the corresponding phosphine oxides, sulfides, and selenides and PB-containing betaines. In the reactions of compound 1 with amines aminoniethylphosphines of the diazaphosphorinane and diazadiphosphacyclooctane series are formed. Ammonium 1,3,2,5-dioxaborataphosphorinanes dissociate in solutions and enter into ion exchange with phosphonium iodides, leading to phosphonium 1,3,2,5-dioxaborataphosphorinanes. The latter. in the case of the aminomethylphosphonium cation, undergo intramolecular rearrangement with the formation of PB-containing betaines and aminomethylphosphines.
  • Synthesis of ammonium 1,3,2,5-dioxaborataphosphorinanes
    作者:B. A. Arbuzov、O. A. Erasmov、G. N. Nikonov、A. A. Karasik
    DOI:10.1007/bf00954832
    日期:1986.7
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