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FcC2C(O)(p-EtPh) | 1198428-26-0

中文名称
——
中文别名
——
英文名称
FcC2C(O)(p-EtPh)
英文别名
——
FcC2C(O)(p-EtPh)化学式
CAS
1198428-26-0
化学式
C21H18FeO
mdl
——
分子量
342.22
InChiKey
UZCCXMBZGZMJKV-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    1,3-二甲基-6-氨基脲嘧啶FcC2C(O)(p-EtPh) 在 nickel (II) cyanide * n H2O CO 、 KCN 作用下, 以 sodium hydroxide 为溶剂, 以72%的产率得到1-p-ethylphenyl-3-methylamino-3-ferrocenyl-2-propenone
    参考文献:
    名称:
    Synthesis of ferrocenyl-β-enamino ketones: A search of ferrocenylpyrido[2,3-d]pyrimidines using a Ni(CN)2/NaOH/KCN system as catalytic precursor
    摘要:
    New ferrocenyl-beta-enamino ketones (1-6), were obtained from 6-amino-1,3-dimethyluracil and several ferrocenyl-alpha-ketoalkynes via MeNH- anion in a monophasic aqueous system containing Ni(CN)(2)/CO/NaOH/H2O/KCN are described. A mechanism for obtaining of beta-enamino ketones is suggested. (C) 2009 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2009.07.017
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文献信息

  • Synthesis of new 7-ferrocenyl-β-enaminone-coumarins and ferrocenyl-pyrano[3,2-g]quinolin-2-ones from coumarin and ferrocenyl-α-ketoalkynes using Ni(CN)2/NaOH/H2O/CO/KCN aqueous catalytic system
    作者:Ivonne Arellano、Pankaj Sharma、Laura Rubio-Perez、Armando Cabrera、Noé Rosas、A. Toscano
    DOI:10.1016/j.jorganchem.2011.11.010
    日期:2012.3
    New ferrocenyl-beta-enaminone-coumarins (1a-5a) and ferrocenyl-pyrano[3,2-g] quinolin-2-ones (1b-5b) were obtained through a heterocyclization reaction from 7-amino-4-methyl-2H-chromen-2-one and several ferrocenyl-alpha-ketoalkynes in a nickel homogeneous aqueous catalytic system formed by Ni(CN)(2)/CO/NaOH/KCN. In the absence of this catalytic system neither ferrocenyl substituted chromenone nor ferrocenyl-heterocycle was obtained. A possible mechanism is suggested for the synthesis of -beta-enaminone-coumarins and pyrano[3,2-g] quinolinones. Molecular structure of 7-(1-ferrocenyl-3-(4-bromophenyl)-3-oxoprop-1-enylamino)-4-methyl-2H-chromen-2-one (5a) has been determined. (C) 2011 Elsevier B. V. All rights reserved.
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