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8-hydroxy-4,8-dimethyl-5-cyanospiro[2.5]oct-4-en-6-one | 1021445-15-7

中文名称
——
中文别名
——
英文名称
8-hydroxy-4,8-dimethyl-5-cyanospiro[2.5]oct-4-en-6-one
英文别名
8-Hydroxy-4,8-dimethyl-6-oxospiro[2.5]oct-4-ene-5-carbonitrile;8-hydroxy-4,8-dimethyl-6-oxospiro[2.5]oct-4-ene-5-carbonitrile
8-hydroxy-4,8-dimethyl-5-cyanospiro[2.5]oct-4-en-6-one化学式
CAS
1021445-15-7
化学式
C11H13NO2
mdl
——
分子量
191.23
InChiKey
FEOQVHVNEOYDBF-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):
    0.2
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    61.1
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    8-hydroxy-4,8-dimethyl-5-cyanospiro[2.5]oct-4-en-6-one三氟化硼乙醚四丁基碘化铵 作用下, 以 二氯甲烷 为溶剂, 反应 12.0h, 以75%的产率得到4-(2-iodoethyl)-3,5-dimethyl-2-cyanophenol
    参考文献:
    名称:
    Synthesis and reactions of functionalized spirocyclopropanes by cyclization of dilithiated β-ketosulfones, α-cyanoacetone and diethyl 2-oxopropylphosphonate with 1,1-diacetylcyclopropane
    摘要:
    The cyclization of beta-ketosulfone, beta-ketonitrile and beta-ketophosphonate dianions with 1,1-diacetylcyclopropane afforded 1-hydroxyspiro[5.2]-cyclooct-4-en-3-ones, which were transformed, by reaction with tetrabutylammonium halides, into functionalized phenols containing a remote halide function. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.01.066
  • 作为产物:
    描述:
    5-甲基异恶唑1,1-乙酰基环丙烷lithium diisopropyl amide 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 15.0h, 以41%的产率得到8-hydroxy-4,8-dimethyl-5-cyanospiro[2.5]oct-4-en-6-one
    参考文献:
    名称:
    Synthesis and reactions of functionalized spirocyclopropanes by cyclization of dilithiated β-ketosulfones, α-cyanoacetone and diethyl 2-oxopropylphosphonate with 1,1-diacetylcyclopropane
    摘要:
    The cyclization of beta-ketosulfone, beta-ketonitrile and beta-ketophosphonate dianions with 1,1-diacetylcyclopropane afforded 1-hydroxyspiro[5.2]-cyclooct-4-en-3-ones, which were transformed, by reaction with tetrabutylammonium halides, into functionalized phenols containing a remote halide function. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.01.066
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文献信息

  • Synthesis and reactions of functionalized spirocyclopropanes by cyclization of dilithiated β-ketosulfones, α-cyanoacetone and diethyl 2-oxopropylphosphonate with 1,1-diacetylcyclopropane
    作者:Nasir Rasool、Muhammad A. Rashid、Helmut Reinke、Christine Fischer、Peter Langer
    DOI:10.1016/j.tet.2008.01.066
    日期:2008.3
    The cyclization of beta-ketosulfone, beta-ketonitrile and beta-ketophosphonate dianions with 1,1-diacetylcyclopropane afforded 1-hydroxyspiro[5.2]-cyclooct-4-en-3-ones, which were transformed, by reaction with tetrabutylammonium halides, into functionalized phenols containing a remote halide function. (c) 2008 Elsevier Ltd. All rights reserved.
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