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2-(3-ethoxyphenyl)pyrimidine | 1529531-15-4

中文名称
——
中文别名
——
英文名称
2-(3-ethoxyphenyl)pyrimidine
英文别名
2-(3-Ethoxyphenyl)pyrimidine
2-(3-ethoxyphenyl)pyrimidine化学式
CAS
1529531-15-4
化学式
C12H12N2O
mdl
——
分子量
200.24
InChiKey
FZRRXCDCNLWLBP-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):
    2.2
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    35
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    3-乙氧基苯甲醛吡啶potassium carbonate 、 sodium hydroxide 作用下, 以 二氯甲烷二甲基亚砜叔丁醇 为溶剂, 反应 7.0h, 生成 2-(3-ethoxyphenyl)pyrimidine
    参考文献:
    名称:
    Efficient and Benign One-Pot Conversion of N-Tosyl-1,4,5,6-tetrahydropyrimidines to Pyrimidines via Tandem β-Elimination and Aromatization
    摘要:
    An efficient, mild, benign, and practical method for one-pot conversion of N-tosyl-1,4,5,6-tetrahydropyrimidines into pyrimidines is discussed in detail. In this method, N-tosyl-1,4,5,6-tetrahydropyrimidines are first prepared via N-tosylation of tetrahydropyrimidines with TsCl and then treated with 1.5 equivalents of NaOH in dimethylsulfoxide (DMSO) under air at 60 degrees C to afford corresponding pyrimidines in 70-95% yields via cascade -elimination and aromatization. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) for the following free supplemental resources: Full experimental and spectral details.]
    DOI:
    10.1080/00397911.2013.764433
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文献信息

  • Efficient and Benign One-Pot Conversion of <i>N</i>-Tosyl-1,4,5,6-tetrahydropyrimidines to Pyrimidines via Tandem <font>β</font>-Elimination and Aromatization
    作者:Tien Ha Trieu、Jing Dong、Xiao-Xin Shi、Xia Lu、Qiang Zhang
    DOI:10.1080/00397911.2013.764433
    日期:2013.12.2
    An efficient, mild, benign, and practical method for one-pot conversion of N-tosyl-1,4,5,6-tetrahydropyrimidines into pyrimidines is discussed in detail. In this method, N-tosyl-1,4,5,6-tetrahydropyrimidines are first prepared via N-tosylation of tetrahydropyrimidines with TsCl and then treated with 1.5 equivalents of NaOH in dimethylsulfoxide (DMSO) under air at 60 degrees C to afford corresponding pyrimidines in 70-95% yields via cascade -elimination and aromatization. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) for the following free supplemental resources: Full experimental and spectral details.]
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