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2-氯-1-环丁基-2,3-二甲基-3-丁烯-1-酮 | 131353-07-6

中文名称
2-氯-1-环丁基-2,3-二甲基-3-丁烯-1-酮
中文别名
3-丁烯-1-酮,2-氯-1-环丁基-2,3-二甲基-(9CI)
英文名称
2-chloro-1-cyclobutyl-3-methyl-3-buten-1-one
英文别名
2-Chloro-1-cyclobutyl-2,3-dimethylbut-3-en-1-one
2-氯-1-环丁基-2,3-二甲基-3-丁烯-1-酮化学式
CAS
131353-07-6
化学式
C10H15ClO
mdl
——
分子量
186.681
InChiKey
NJHWQWRNZFCQTG-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

物化性质

  • 沸点:
    252.6±20.0 °C(Predicted)
  • 密度:
    1.069±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:4b6599c4edb94d7a937c5a71b8bb64e2
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反应信息

  • 作为反应物:
    描述:
    2-氯-1-环丁基-2,3-二甲基-3-丁烯-1-酮双(三甲基硅烷基)氨基钾 作用下, 以 四氢呋喃六甲基磷酰三胺 为溶剂, 以52%的产率得到6,7-dimethylspiro<3.4>oct-6-en-5-one
    参考文献:
    名称:
    Base-induced cyclization of .alpha.-chloro .beta.,.gamma.-unsaturated ketones : facile synthesis of tri- and tetrasubstituted 2-cyclopenten-1-ones
    摘要:
    Base-induced cyclization of fully substituted alpha-chloro beta,gamma-unsaturated ketones results in substituted cyclopentenones. Potassium tert-butoxide, lithium diisopropylamide, sodium hydroxide, and ammonium hydroxide can be used as the base for this process. In the case of ammonium hydroxide, it is proposed that initial formation of an enamine is followed by an intramolecular S(N)2' reaction of the enamine carbon. For all other bases, the reaction most likely proceeds through a ketone enolate. Application of this novel cyclization has been extended to the synthesis of several 2,3-disubstituted, 2,3,5-trisubstituted, and 2,3,5-tetrasubstituted 2-cyclopenten-1-ones.
    DOI:
    10.1021/jo00002a042
  • 作为产物:
    描述:
    参考文献:
    名称:
    Base-induced cyclization of .alpha.-chloro .beta.,.gamma.-unsaturated ketones : facile synthesis of tri- and tetrasubstituted 2-cyclopenten-1-ones
    摘要:
    Base-induced cyclization of fully substituted alpha-chloro beta,gamma-unsaturated ketones results in substituted cyclopentenones. Potassium tert-butoxide, lithium diisopropylamide, sodium hydroxide, and ammonium hydroxide can be used as the base for this process. In the case of ammonium hydroxide, it is proposed that initial formation of an enamine is followed by an intramolecular S(N)2' reaction of the enamine carbon. For all other bases, the reaction most likely proceeds through a ketone enolate. Application of this novel cyclization has been extended to the synthesis of several 2,3-disubstituted, 2,3,5-trisubstituted, and 2,3,5-tetrasubstituted 2-cyclopenten-1-ones.
    DOI:
    10.1021/jo00002a042
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文献信息

  • MATHEW, JACOB, J. ORG. CHEM., 56,(1991) N, C. 713-716
    作者:MATHEW, JACOB
    DOI:——
    日期:——
  • Base-induced cyclization of .alpha.-chloro .beta.,.gamma.-unsaturated ketones : facile synthesis of tri- and tetrasubstituted 2-cyclopenten-1-ones
    作者:Jacob Mathew
    DOI:10.1021/jo00002a042
    日期:1991.1
    Base-induced cyclization of fully substituted alpha-chloro beta,gamma-unsaturated ketones results in substituted cyclopentenones. Potassium tert-butoxide, lithium diisopropylamide, sodium hydroxide, and ammonium hydroxide can be used as the base for this process. In the case of ammonium hydroxide, it is proposed that initial formation of an enamine is followed by an intramolecular S(N)2' reaction of the enamine carbon. For all other bases, the reaction most likely proceeds through a ketone enolate. Application of this novel cyclization has been extended to the synthesis of several 2,3-disubstituted, 2,3,5-trisubstituted, and 2,3,5-tetrasubstituted 2-cyclopenten-1-ones.
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