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2-(1-chloro-2-methylpropyl)-5-methylfuran | 917769-50-7

中文名称
——
中文别名
——
英文名称
2-(1-chloro-2-methylpropyl)-5-methylfuran
英文别名
2-(1-Chloro-2-methylpropyl)-5-methylfuran
2-(1-chloro-2-methylpropyl)-5-methylfuran化学式
CAS
917769-50-7
化学式
C9H13ClO
mdl
——
分子量
172.655
InChiKey
CFDMKRJAGKCSOO-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:
    182.1±25.0 °C(Predicted)
  • 密度:
    1.034±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    13.1
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:b79353486331d772a8b5923de7023edf
查看

反应信息

  • 作为反应物:
    描述:
    2-(1-chloro-2-methylpropyl)-5-methylfuransodium diethyl phosphite 为溶剂, 反应 9.5h, 以48%的产率得到2-(1-diethoxyphosphoryl-2-methylpropyl)-5-methylfuran
    参考文献:
    名称:
    2-(1-Chloroalkyl)furans in the reaction with sodium diethyl phosphite
    摘要:
    2-(1-Chloroethyl) and 2-(1-chloro-2-methylpropyl)furans react with sodium diethyl phosphite to give two products, 2-(1-diethoxyphosphorylmethyl)furan and 2-alkyl-5-(diethoxyphosphoryloxy)furan. The fraction of the latter product increases with increasing size of the alkyl radical. 2-Methyl substitution in the substrate completely suppresses phosphate formation. 2-(1-Chloroethyl)-5-(2-methylpropyl)furan under the action of sodium diethyl phosphite eliminates hydrogen chloride to give the corresponding alkene.
    DOI:
    10.1134/s1070363206040207
  • 作为产物:
    描述:
    2-methyl-1-(5-methylfuran-2-yl)propan-1-ol吡啶氯化亚砜 作用下, 以 乙醚 为溶剂, 以49%的产率得到2-(1-chloro-2-methylpropyl)-5-methylfuran
    参考文献:
    名称:
    2-(1-Chloroalkyl)furans in the reaction with sodium diethyl phosphite
    摘要:
    2-(1-Chloroethyl) and 2-(1-chloro-2-methylpropyl)furans react with sodium diethyl phosphite to give two products, 2-(1-diethoxyphosphorylmethyl)furan and 2-alkyl-5-(diethoxyphosphoryloxy)furan. The fraction of the latter product increases with increasing size of the alkyl radical. 2-Methyl substitution in the substrate completely suppresses phosphate formation. 2-(1-Chloroethyl)-5-(2-methylpropyl)furan under the action of sodium diethyl phosphite eliminates hydrogen chloride to give the corresponding alkene.
    DOI:
    10.1134/s1070363206040207
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