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5-(3,4-dimethoxyphenyl)-5-methyl-3-(1-naphthyl)-4,5-dihydro-1,2-oxazole

中文名称
——
中文别名
——
英文名称
5-(3,4-dimethoxyphenyl)-5-methyl-3-(1-naphthyl)-4,5-dihydro-1,2-oxazole
英文别名
5-(3,4-dimethoxyphenyl)-5-methyl-3-naphthalen-1-yl-4H-1,2-oxazole
5-(3,4-dimethoxyphenyl)-5-methyl-3-(1-naphthyl)-4,5-dihydro-1,2-oxazole化学式
CAS
——
化学式
C22H21NO3
mdl
——
分子量
347.414
InChiKey
XMUAWBHYMPMGAO-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):
    4.7
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    40
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1-(1-萘)-乙酮肟3,4-二甲氧基苯乙酮lithium diisopropyl amide盐酸 作用下, 以 四氢呋喃 为溶剂, 以48%的产率得到5-(3,4-dimethoxyphenyl)-5-methyl-3-(1-naphthyl)-4,5-dihydro-1,2-oxazole
    参考文献:
    名称:
    The Preparation of 5-Aryl-5-methyl-4,5-dihydroisoxazoles from Dilithiated C(α), O -Oximes and Select Acetyl Ketones
    摘要:
    Several 5-aryl-5-methyl-4,5-dihydroisoxazoles were prepared by a three-step, one-pot process in 24-83% yield. C(alpha),O-oximes were dilithiated with lithium diisopropylamide and condensed with electron enriched acetophenones, such as 4'-methoxyacetophenone, followed by immediate acid cyclization.
    DOI:
    10.1081/scc-120026359
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文献信息

  • The Preparation of 5-Aryl-5-methyl-4,5-dihydroisoxazoles from Dilithiated C(α),<b> <i>O</i> </b>-Oximes and Select Acetyl Ketones
    作者:Matthew J. Walters、S. Patrick Dunn、Emily Choi、Amanda N. D'Elia、Morgan E. Warner、Charles F. Beam
    DOI:10.1081/scc-120026359
    日期:2003.12.1
    Several 5-aryl-5-methyl-4,5-dihydroisoxazoles were prepared by a three-step, one-pot process in 24-83% yield. C(alpha),O-oximes were dilithiated with lithium diisopropylamide and condensed with electron enriched acetophenones, such as 4'-methoxyacetophenone, followed by immediate acid cyclization.
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