摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4-(1-hydroxyethyl)cyclohept-4-enone | 278603-91-1

中文名称
——
中文别名
——
英文名称
4-(1-hydroxyethyl)cyclohept-4-enone
英文别名
4-(1-Hydroxyethyl)-4-cyclohepten-1-one;4-(1-hydroxyethyl)cyclohept-4-en-1-one
4-(1-hydroxyethyl)cyclohept-4-enone化学式
CAS
278603-91-1
化学式
C9H14O2
mdl
——
分子量
154.209
InChiKey
JLCNHAUVNZFHCG-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):
    0.1
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    3-丁炔-2-醇1-乙烯基-1-(2-甲氧基乙氧基)环丙烷 在 di(rhodium)tetracarbonyl dichloride 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 0.2h, 以89%的产率得到4-(1-hydroxyethyl)cyclohept-4-enone
    参考文献:
    名称:
    A New and Practical Five-Carbon Component for Metal-Catalyzed [5 + 2] Cycloadditions:  Preparative Scale Syntheses of Substituted Cycloheptenones
    摘要:
    Described herein is an efficient preparative scale synthesis of 1-(2-methyoxyethoxy)-1-vinylcyclopropane and the investigation of the utility of this reagent as a new five-carbon component in metal-catalyzed [5 + 2] cycloadditions. A new cycloaddition procedure is also described that proceeds up to 12-fold faster and with 10-fold less catalyst than previously described, providing cycloheptenones in many cases in minutes and in isolated yields of 75-97%. The procedure is readily conducted on a small or large scale (up to 100 mmol thus far).
    DOI:
    10.1021/ol0058691
点击查看最新优质反应信息

文献信息

  • A New and Practical Five-Carbon Component for Metal-Catalyzed [5 + 2] Cycloadditions:  Preparative Scale Syntheses of Substituted Cycloheptenones
    作者:Paul A. Wender、Alaric J. Dyckman、Craig O. Husfeld、Marc J. C. Scanio
    DOI:10.1021/ol0058691
    日期:2000.6.1
    Described herein is an efficient preparative scale synthesis of 1-(2-methyoxyethoxy)-1-vinylcyclopropane and the investigation of the utility of this reagent as a new five-carbon component in metal-catalyzed [5 + 2] cycloadditions. A new cycloaddition procedure is also described that proceeds up to 12-fold faster and with 10-fold less catalyst than previously described, providing cycloheptenones in many cases in minutes and in isolated yields of 75-97%. The procedure is readily conducted on a small or large scale (up to 100 mmol thus far).
  • THE PREPARATION OF CYCLOHEPT-4-ENONES BY RHODIUM-CATALYZED INTERMOLECULAR [5+2] CYCLOADDITION
    作者:Wender, Paul A.、Lesser, Adam B.、Sirois, Lauren E.
    DOI:10.15227/orgsyn.088.0109
    日期:——
查看更多