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(Z)-5-(4-methoxyphenyl)-2,3-dipropyl-2-penten-4-ynenitrile | 1011718-05-0

中文名称
——
中文别名
——
英文名称
(Z)-5-(4-methoxyphenyl)-2,3-dipropyl-2-penten-4-ynenitrile
英文别名
(Z)-3-(4-methoxyphenyl)ethynyl-2-propylhex-2-enenitrile;(Z)-3-[2-(4-methoxyphenyl)ethynyl]-2-propylhex-2-enenitrile
(Z)-5-(4-methoxyphenyl)-2,3-dipropyl-2-penten-4-ynenitrile化学式
CAS
1011718-05-0
化学式
C18H21NO
mdl
——
分子量
267.371
InChiKey
VIODSKNRAMCXNT-MSUUIHNZSA-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):
    5.4
  • 重原子数:
    20
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    33
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    4-辛炔3-(4-methoxyphenyl)propiolonitrilebis(1,5-cyclooctadiene)nickel (0)三苯基硼烷4,5-双二苯基膦-9,9-二甲基氧杂蒽 作用下, 以 十四烷甲苯 为溶剂, 反应 2.0h, 以68%的产率得到(Z)-5-(4-methoxyphenyl)-2,3-dipropyl-2-penten-4-ynenitrile
    参考文献:
    名称:
    Alkynylcyanation of alkynes and dienes catalyzed by nickel
    摘要:
    Alkynyl cyanides are found to add across alkynes and 1,2-dienes in the presence of a catalyst prepared in situ from Ni(cod)(2), xantphos, and BPh3. A range of functionalized conjugated cis-enynes are obtained with high regioselectivity. The addition reaction across norbornadiene proceeds in the absence of BPh3 to give exo-cis adduct exclusively. A stoichiometric reaction of ail alkynyl cyanide, Ni(cod)2, xantphos, and BPh3 gives trans-(xantphos)Ni(CNBPh3)(C CSiMe(2)t-Bu), which is suggested to be a plausible reaction intermediate of the alkynylcyanation reaction. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.03.079
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文献信息

  • Nickel/BPh3-Catalyzed Alkynylcyanation of Alkynes and 1,2-Dienes: An Efficient Route to Highly Functionalized Conjugated Enynes
    作者:Yoshiaki Nakao、Yasuhiro Hirata、Masaaki Tanaka、Tamejiro Hiyama
    DOI:10.1002/anie.200704095
    日期:2008.1
  • Alkynylcyanation of alkynes and dienes catalyzed by nickel
    作者:Yasuhiro Hirata、Masaaki Tanaka、Akira Yada、Yoshiaki Nakao、Tamejiro Hiyama
    DOI:10.1016/j.tet.2009.03.079
    日期:2009.6
    Alkynyl cyanides are found to add across alkynes and 1,2-dienes in the presence of a catalyst prepared in situ from Ni(cod)(2), xantphos, and BPh3. A range of functionalized conjugated cis-enynes are obtained with high regioselectivity. The addition reaction across norbornadiene proceeds in the absence of BPh3 to give exo-cis adduct exclusively. A stoichiometric reaction of ail alkynyl cyanide, Ni(cod)2, xantphos, and BPh3 gives trans-(xantphos)Ni(CNBPh3)(C CSiMe(2)t-Bu), which is suggested to be a plausible reaction intermediate of the alkynylcyanation reaction. (C) 2009 Elsevier Ltd. All rights reserved.
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