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4-methyl-2-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)pent-4-en-2-ol | 1433220-35-9

中文名称
——
中文别名
——
英文名称
4-methyl-2-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)pent-4-en-2-ol
英文别名
4-Methyl-2-[4-(oxan-2-yloxy)phenyl]pent-4-en-2-ol;4-methyl-2-[4-(oxan-2-yloxy)phenyl]pent-4-en-2-ol
4-methyl-2-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)pent-4-en-2-ol化学式
CAS
1433220-35-9
化学式
C17H24O3
mdl
——
分子量
276.376
InChiKey
FKNAECHIGQAAEP-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):
    3.8
  • 重原子数:
    20
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    38.7
  • 氢给体数:
    1
  • 氢受体数:
    3

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:
    1-[4-[(四氢-2H-吡喃-2-基)氧基]苯基]乙酮B-2-(2-methylallyl)-1,3,2-dioxaborinane2-甲基-2-丁醇 作用下, 以 neat (no solvent) 为溶剂, 以91%的产率得到4-methyl-2-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)pent-4-en-2-ol
    参考文献:
    名称:
    Solvent-Free Methallylboration of Ketones Accelerated by tert-Alcohols
    摘要:
    A solvent- and metal-free process has been developed for the direct methallylboration of ketones employing the stable B-methallylborinane 1, which was accelerated by tertiary alcohols. In the presence of 2.0 equiv of readily available tertiary alcohols such as tert-amyl alcohol, the methallylation products were prepared at room temperature in excellent yields. The salient features of the described process include simple operation, high efficiency, and mild reaction conditions.
    DOI:
    10.1021/jo4006574
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文献信息

  • Solvent-Free Methallylboration of Ketones Accelerated by <i>tert</i>-Alcohols
    作者:Yongda Zhang、Ning Li、Navneet Goyal、Guisheng Li、Heewon Lee、Bruce Z. Lu、Chris H. Senanayake
    DOI:10.1021/jo4006574
    日期:2013.6.7
    A solvent- and metal-free process has been developed for the direct methallylboration of ketones employing the stable B-methallylborinane 1, which was accelerated by tertiary alcohols. In the presence of 2.0 equiv of readily available tertiary alcohols such as tert-amyl alcohol, the methallylation products were prepared at room temperature in excellent yields. The salient features of the described process include simple operation, high efficiency, and mild reaction conditions.
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