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(+/-)-1-n-butoxy-8-hydroxy-2-oxo-1,2-dihydronaphthalene-1-carbonitrile | 1173286-15-1

中文名称
——
中文别名
——
英文名称
(+/-)-1-n-butoxy-8-hydroxy-2-oxo-1,2-dihydronaphthalene-1-carbonitrile
英文别名
1-Butoxy-8-hydroxy-2-oxonaphthalene-1-carbonitrile;1-butoxy-8-hydroxy-2-oxonaphthalene-1-carbonitrile
(+/-)-1-n-butoxy-8-hydroxy-2-oxo-1,2-dihydronaphthalene-1-carbonitrile化学式
CAS
1173286-15-1
化学式
C15H15NO3
mdl
——
分子量
257.289
InChiKey
MLHRWMPAGDGJGG-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):
    2.5
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    70.3
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    (+/-)-3a-n-butoxynaphtho[1,8-de][1,2]oxazin-4(3aH)-oneN,N-二甲基甲酰胺 为溶剂, 反应 0.07h, 以84%的产率得到(+/-)-1-n-butoxy-8-hydroxy-2-oxo-1,2-dihydronaphthalene-1-carbonitrile
    参考文献:
    名称:
    Novel Thermal and Microwave-Assisted Facile Route to Naphthalen-2(1H)-ones via an Oxidative Alkoxylation-Ring-Opening Protocol
    摘要:
    Several novel 1,1-disubstituted-8-hydroxynaphthalen-2(1H)-ones have been efficiently synthesized via a two-step sequence from 2-hydroxy-1-naphthaldehyde oxime. The methodology involves oxidative ring closure and alkoxylation to 3a-alkoxynaphtho[1,8-de][1,2]oxazin-4(3aH)-ones, followed by thermal ring-opening. Both thermal and microwave irradiation conditions were used. A novel one-pot reaction of oxime to 8-isopropoxynaphthalene-1,7-diol using microwave irradiation is also reported.
    DOI:
    10.1021/ol9008574
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文献信息

  • Novel Thermal and Microwave-Assisted Facile Route to Naphthalen-2(1<i>H</i>)-ones via an Oxidative Alkoxylation-Ring-Opening Protocol
    作者:Chrysanthi Dolka、Kristof Van Hecke、Luc Van Meervelt、Petros G. Tsoungas、Erik V. Van der Eycken、George Varvounis
    DOI:10.1021/ol9008574
    日期:2009.7.16
    Several novel 1,1-disubstituted-8-hydroxynaphthalen-2(1H)-ones have been efficiently synthesized via a two-step sequence from 2-hydroxy-1-naphthaldehyde oxime. The methodology involves oxidative ring closure and alkoxylation to 3a-alkoxynaphtho[1,8-de][1,2]oxazin-4(3aH)-ones, followed by thermal ring-opening. Both thermal and microwave irradiation conditions were used. A novel one-pot reaction of oxime to 8-isopropoxynaphthalene-1,7-diol using microwave irradiation is also reported.
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