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1-(3,6-二氢-2H-吡喃-4-基)乙酮 | 405910-68-1

中文名称
1-(3,6-二氢-2H-吡喃-4-基)乙酮
中文别名
——
英文名称
1-(3,6-Dihydro-2H-pyran-4-yl)-ethanone
英文别名
1-(3,6-Dihydro-2H-pyran-4-yl)ethan-1-one;1-(3,6-dihydro-2H-pyran-4-yl)ethanone
1-(3,6-二氢-2H-吡喃-4-基)乙酮化学式
CAS
405910-68-1
化学式
C7H10O2
mdl
——
分子量
126.155
InChiKey
KDWKXQAAHXFYFX-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:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    (4-Allyloxy-but-1-ynyloxy)-triisopropyl-silane 在 [(N,N-(MeSO2)2-imidazolidin-2-yl)RuCl2(PCy3)=CHPh] 、 氢氟酸 作用下, 以 乙腈 为溶剂, 反应 1.5h, 以88%的产率得到1-(3,6-二氢-2H-吡喃-4-基)乙酮
    参考文献:
    名称:
    Siloxyalkyne–Alkene Metathesis: Rapid Access to Highly Functionalized Enones
    摘要:
    Mechanistically intriguing participation of siloxyalkynes occurs in the intramolecular Ru-catalyzed metathesis with terminal alkenes (see scheme; Ms=methanesulfonyl). Combined with efficient protodesilylation, this process resulted in the development of a new method for the synthesis of highly functionalized enones starting from readily accessible acyclic precursors. Heterocyclic and polycyclic compounds were prepared efficiently, which illustrates the generality of this novel method.
    DOI:
    10.1002/1521-3773(20011119)40:22<4274::aid-anie4274>3.0.co;2-#
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文献信息

  • THIAZOLE DERIVATIVES
    申请人:Kyowa Hakko Kirin Co., Ltd.
    公开号:EP3002283B1
    公开(公告)日:2017-06-14
  • Siloxyalkyne–Alkene Metathesis: Rapid Access to Highly Functionalized Enones
    作者:Michael P. Schramm、D. Srinivasa Reddy、Sergey A. Kozmin
    DOI:10.1002/1521-3773(20011119)40:22<4274::aid-anie4274>3.0.co;2-#
    日期:2001.11.19
    Mechanistically intriguing participation of siloxyalkynes occurs in the intramolecular Ru-catalyzed metathesis with terminal alkenes (see scheme; Ms=methanesulfonyl). Combined with efficient protodesilylation, this process resulted in the development of a new method for the synthesis of highly functionalized enones starting from readily accessible acyclic precursors. Heterocyclic and polycyclic compounds were prepared efficiently, which illustrates the generality of this novel method.
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