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[(3aR,5R,6S,6aR)-5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-6-yl] 4,4-dimethyl-2-oxocyclopentane-1-carboxylate | 1093076-55-1

中文名称
——
中文别名
——
英文名称
[(3aR,5R,6S,6aR)-5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-6-yl] 4,4-dimethyl-2-oxocyclopentane-1-carboxylate
英文别名
——
[(3aR,5R,6S,6aR)-5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-6-yl] 4,4-dimethyl-2-oxocyclopentane-1-carboxylate化学式
CAS
1093076-55-1
化学式
C20H30O8
mdl
——
分子量
398.453
InChiKey
SLGHRCPMFPVPGA-YGPORJGJSA-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):
    1.8
  • 重原子数:
    28
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    89.5
  • 氢给体数:
    0
  • 氢受体数:
    8

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    2-重氮基-5,5-二甲基-1,3-环己二酮双丙酮葡萄糖甲苯 为溶剂, 180.0 ℃ 、1.7 MPa 条件下, 反应 0.1h, 以55%的产率得到[(3aR,5R,6S,6aR)-5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-6-yl] 4,4-dimethyl-2-oxocyclopentane-1-carboxylate
    参考文献:
    名称:
    Microwave-Assisted Wolff Rearrangement of Cyclic 2-Diazo-1,3-Diketones: An Eco-compatible Route to α-Carbonylated Cycloalkanones
    摘要:
    The microwave-assisted Wolff rearrangement of cyclic 2-diazo-1.3-diketones performed in the presence of a stoichiometric amount of alcohol, amine, or thiol is an efficient, user, and environmentally friendly synthetic protocol for the synthesis of alpha-carbonylated cycloalkanones. This approach proves superior to existing protocols in scope and eco-compatibility.
    DOI:
    10.1021/jo8021567
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文献信息

  • Microwave-Assisted Wolff Rearrangement of Cyclic 2-Diazo-1,3-Diketones: An Eco-compatible Route to α-Carbonylated Cycloalkanones
    作者:Marc Presset、Yoann Coquerel、Jean Rodriguez
    DOI:10.1021/jo8021567
    日期:2009.1.2
    The microwave-assisted Wolff rearrangement of cyclic 2-diazo-1.3-diketones performed in the presence of a stoichiometric amount of alcohol, amine, or thiol is an efficient, user, and environmentally friendly synthetic protocol for the synthesis of alpha-carbonylated cycloalkanones. This approach proves superior to existing protocols in scope and eco-compatibility.
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