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1-(tert-butoxyformamido)-2,2-dibromo-1-(naphthalen-1-yl)-2-nitroethane | 1420742-81-9

中文名称
——
中文别名
——
英文名称
1-(tert-butoxyformamido)-2,2-dibromo-1-(naphthalen-1-yl)-2-nitroethane
英文别名
tert-butyl N-(2,2-dibromo-1-naphthalen-1-yl-2-nitroethyl)carbamate
1-(tert-butoxyformamido)-2,2-dibromo-1-(naphthalen-1-yl)-2-nitroethane化学式
CAS
1420742-81-9
化学式
C17H18Br2N2O4
mdl
——
分子量
474.149
InChiKey
KRCDJNJZEZXRBX-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):
    5.1
  • 重原子数:
    25
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    84.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Approach to Vicinal t-Boc-amino Dibromides via Catalytic Aminobromination of Nitrostyrenes without Using Chromatography and Recrystallization
    摘要:
    A 1.0 mol % amount of K3PO4 center dot 3H(2)O was found to catalyze aminohalogenation reaction of nitrostyrenes with N,N-dibromo-tert-butylcarbamate (t-Boc-NBr2) in a dichloroethane system. Good to excellent yields and complete regioselectivity have been achieved by taking advantage of the GAP workup without using traditional purification techniques such as column chromatography and recrystallization. A new mechanism is proposed involving radical and ionic catalytic cycles and an intramolecular migration.
    DOI:
    10.1021/jo302727v
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文献信息

  • Approach to Vicinal <i>t</i>-Boc-amino Dibromides via Catalytic Aminobromination of Nitrostyrenes without Using Chromatography and Recrystallization
    作者:Hao Sun、Jianlin Han、Padmanabha V. Kattamuri、Yi Pan、Guigen Li
    DOI:10.1021/jo302727v
    日期:2013.2.1
    A 1.0 mol % amount of K3PO4 center dot 3H(2)O was found to catalyze aminohalogenation reaction of nitrostyrenes with N,N-dibromo-tert-butylcarbamate (t-Boc-NBr2) in a dichloroethane system. Good to excellent yields and complete regioselectivity have been achieved by taking advantage of the GAP workup without using traditional purification techniques such as column chromatography and recrystallization. A new mechanism is proposed involving radical and ionic catalytic cycles and an intramolecular migration.
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