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1,2-bis(3-hydroxy-3-phenyl-1-propynyl)benzene | 880362-22-1

中文名称
——
中文别名
——
英文名称
1,2-bis(3-hydroxy-3-phenyl-1-propynyl)benzene
英文别名
3-[2-(3-Hydroxy-3-phenylprop-1-ynyl)phenyl]-1-phenylprop-2-yn-1-ol
1,2-bis(3-hydroxy-3-phenyl-1-propynyl)benzene化学式
CAS
880362-22-1
化学式
C24H18O2
mdl
——
分子量
338.406
InChiKey
QPCBBXFZBSEROH-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):
    4.3
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1,2-bis(3-hydroxy-3-phenyl-1-propynyl)benzene二苯基氯化膦三乙胺 作用下, 以 四氢呋喃 为溶剂, 反应 4.0h, 以87%的产率得到3,8-Bis-(diphenyl-phosphinoyl)-1,2-diphenyl-1,2-dihydro-cyclobuta[b]naphthalene
    参考文献:
    名称:
    由1,2-双(3-丙炔醇)苯合成萘[ b ]环丁烯
    摘要:
    我们已经证明,苯桥双(炔丙基醇)与氯二烷基膦的反应通过1,2-双(α-)的[2 + 2]环加成反应独家提供了3,8-双(二​​烷基次膦基)萘[ b ]环丁烯。膦基烯丙基)苯。还已经实现了产物的去磷酸化。
    DOI:
    10.1016/j.tetlet.2005.12.121
  • 作为产物:
    描述:
    1,2-二碘苯(+/-)-1-苯基-2-丙炔-1-醇 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide 二异丙胺 作用下, 以 四氢呋喃 为溶剂, 反应 16.0h, 以96%的产率得到1,2-bis(3-hydroxy-3-phenyl-1-propynyl)benzene
    参考文献:
    名称:
    Reaction of ene-bis(phosphinylallenes): [2+2] versus [4+2] cycloaddition
    摘要:
    Reaction of ene-bis(phosphinylallenes), derived from ene-bis(propargyl alcohols) and chlorodiphenylphosphine, was investigated. Benzene-bridged bis(phosphinylallenes) exclusively gave intramolecular [2+2] cycloadducts in the presence of dimethyl fumarate in sharp contrast to the reaction of benzene-bridged bis(sulfinylallenes), which gave the corresponding [4+2] cycloadducts. On the other hand, substituted ethylene- or five-membered heterocycle-bridged bis(phosphinylallenes) provided [4+2] cycloadducts. Reaction of benzene-bridged diallene bearing both a sulfinyl group and a phosphinyl group on the two allenyl groups was also described. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2006.08.083
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文献信息

  • Reaction of ene-bis(phosphinylallenes): [2+2] versus [4+2] cycloaddition
    作者:Shinji Kitagaki、Yuki Okumura、Chisato Mukai
    DOI:10.1016/j.tet.2006.08.083
    日期:2006.10
    Reaction of ene-bis(phosphinylallenes), derived from ene-bis(propargyl alcohols) and chlorodiphenylphosphine, was investigated. Benzene-bridged bis(phosphinylallenes) exclusively gave intramolecular [2+2] cycloadducts in the presence of dimethyl fumarate in sharp contrast to the reaction of benzene-bridged bis(sulfinylallenes), which gave the corresponding [4+2] cycloadducts. On the other hand, substituted ethylene- or five-membered heterocycle-bridged bis(phosphinylallenes) provided [4+2] cycloadducts. Reaction of benzene-bridged diallene bearing both a sulfinyl group and a phosphinyl group on the two allenyl groups was also described. (c) 2006 Elsevier Ltd. All rights reserved.
  • Synthesis of naphtho[b]cyclobutenes from 1,2-bis(3-propynol)benzenes
    作者:Shinji Kitagaki、Yuki Okumura、Chisato Mukai
    DOI:10.1016/j.tetlet.2005.12.121
    日期:2006.3
    We have demonstrated that the reaction of benzene-bridged bis(propargyl alcohol)s with chlorodialkylphosphines exclusively afforded 3,8-bis(dialkylphosphinyl)naphtho[b]cyclobutenes via the [2+2] cycloaddition of 1,2-bis(α-phosphinylallenyl)benzenes. Dephosphinylation of the product has also been achieved.
    我们已经证明,苯桥双(炔丙基醇)与氯二烷基膦的反应通过1,2-双(α-)的[2 + 2]环加成反应独家提供了3,8-双(二​​烷基次膦基)萘[ b ]环丁烯。膦基烯丙基)苯。还已经实现了产物的去磷酸化。
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