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5--3,4-bis(methylbutyl)-1H-pyrrole-2-carbonitrile | 132699-41-3

中文名称
——
中文别名
——
英文名称
5--3,4-bis(methylbutyl)-1H-pyrrole-2-carbonitrile
英文别名
5-(bis(trimethylsilyl)amino)-3,4-bis(methylbutyl)-1H-pyrrole-2-carbonitrile;5-[bis(trimethylsilyl)amino]-3,4-bis(3-methylbutyl)-1H-pyrrole-2-carbonitrile
5-<bis(trimethylsilyl)amino>-3,4-bis(methylbutyl)-1H-pyrrole-2-carbonitrile化学式
CAS
132699-41-3
化学式
C21H41N3Si2
mdl
——
分子量
391.748
InChiKey
LOQXXWCGBAESGP-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

  • 熔点:
    76-78 °C(Solvent: Hexane)
  • 沸点:
    445.1±55.0 °C(Predicted)
  • 密度:
    0.93±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.54
  • 重原子数:
    26
  • 可旋转键数:
    9
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.76
  • 拓扑面积:
    42.8
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    三甲基氰硅烷2,9-二甲基-5-癸炔carbon monoxide,cobalt,cyclopenta-1,3-diene 作用下, 反应 20.0h, 以92%的产率得到5--3,4-bis(methylbutyl)-1H-pyrrole-2-carbonitrile
    参考文献:
    名称:
    A new method for the construction of the pyrrole ring by the carbonylcobalt-catalyzed reaction of trimethylsilyl cyanide with acetylenes. Its scope and limitations
    摘要:
    The carbonylcobalt-catalyzed reaction of acetylenes with trimethylsilyl cyanide (1) to give 5-amino-1H-pyrrole-2-carbonitriles is described. Reaction of the symmetric internal acetylenes, 4-octyne (2a) and 2,9-dimethyl-5-decyne (2b), with 1 in the presence of a cobalt complex gave 3a and 3b, respectively, in high yield. From unsymmetric acetylenes were obtained mixtures of regioisomeric pyrroles. The regioisomeric ratio depended on the substitution pattern of the acetylenes and on the kind of substituents possessed by the acetylenes. In the case of the internal unsymmetric acetylenes, 2c-2f, isomers in which the bulkier of the two substituents appeared at the 4-position of the pyrrole ring were obtained as the main products. However, the reaction of internal acetylenes bearing an ester group (2g and 2h) gave a reversed selectively. In case of the terminal acetylenes, 1-octyne (2k), 21, and 2m, isomers in which the alkyl group was located at the 3-position of the pyrrole ring were obtained highly selectively. A new cobalt complex (8), prepared by the reaction of CO2(CO)8 with excess 1, catalyzed the formation of pyrrole 3a from 2a and 1. The stoichiometric reaction of complex 8 with 2a also gave 3a in a good yield.
    DOI:
    10.1021/jo00006a038
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文献信息

  • CHATANI, NAOTO;HANAFUSA, TERUKIYO, J. ORG. CHEM., 56,(1991) N, C. 2166-2170
    作者:CHATANI, NAOTO、HANAFUSA, TERUKIYO
    DOI:——
    日期:——
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