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2-(1-azidocyclohexyl)furan | 235787-72-1

中文名称
——
中文别名
——
英文名称
2-(1-azidocyclohexyl)furan
英文别名
——
2-(1-azidocyclohexyl)furan化学式
CAS
235787-72-1
化学式
C10H13N3O
mdl
——
分子量
191.233
InChiKey
PBZLZFRARXNYDU-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):
    3.5
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    27.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2-(1-azidocyclohexyl)furan 在 palladium on activated charcoal sodium azide 、 氢气sodium acetate三乙胺间氯过氧苯甲酸 作用下, 以 甲醇二氯甲烷溶剂黄146乙酸乙酯 为溶剂, 10.0~20.0 ℃ 、100.0 kPa 条件下, 反应 3.67h, 生成 3-amino-1-(4-tolylsulfonyl)-1-azaspiro[5.5]undec-3-ene-2,5-dione
    参考文献:
    名称:
    1,4-Reductive Addition of Hydrazoic Acid to γ-Oxo-α,β-unsaturated δ-Lactones and -Lactams: A Convenient Route to α-Amino-γ-oxo-α,β-unsaturated δ-Lactones and -Lactams
    摘要:
    gamma-Oxo-alpha,beta-unsaturated delta-lactones and lactams, which are easily accessible from their corresponding 2-furylcarbinols, were used as substrates for the 1,4-reductive addition of hydrazoic acid. The outcome of the reaction is the formation, in high yields, of the corresponding alpha-amino-gamma-oxo-alpha,beta-unsaturated delta-lactones and -lactams, compounds of great biological and synthetic interest.
    DOI:
    10.1002/(sici)1099-0690(199906)1999:6<1449::aid-ejoc1449>3.0.co;2-9
  • 作为产物:
    描述:
    1-(2-furyl)cyclohexan-1-ol迭氮酸硫酸 作用下, 以 为溶剂, 反应 1.0h, 以93%的产率得到2-(1-azidocyclohexyl)furan
    参考文献:
    名称:
    1,4-Reductive Addition of Hydrazoic Acid to γ-Oxo-α,β-unsaturated δ-Lactones and -Lactams: A Convenient Route to α-Amino-γ-oxo-α,β-unsaturated δ-Lactones and -Lactams
    摘要:
    gamma-Oxo-alpha,beta-unsaturated delta-lactones and lactams, which are easily accessible from their corresponding 2-furylcarbinols, were used as substrates for the 1,4-reductive addition of hydrazoic acid. The outcome of the reaction is the formation, in high yields, of the corresponding alpha-amino-gamma-oxo-alpha,beta-unsaturated delta-lactones and -lactams, compounds of great biological and synthetic interest.
    DOI:
    10.1002/(sici)1099-0690(199906)1999:6<1449::aid-ejoc1449>3.0.co;2-9
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