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4-[2-(4-bromo-phenyl)-vinyl]-5-chloro-2,3-dihydrobenzo[b]oxepine | 1131454-79-9

中文名称
——
中文别名
——
英文名称
4-[2-(4-bromo-phenyl)-vinyl]-5-chloro-2,3-dihydrobenzo[b]oxepine
英文别名
4-[(E)-2-(4-bromophenyl)ethenyl]-5-chloro-2,3-dihydro-1-benzoxepine
4-[2-(4-bromo-phenyl)-vinyl]-5-chloro-2,3-dihydrobenzo[b]oxepine化学式
CAS
1131454-79-9
化学式
C18H14BrClO
mdl
——
分子量
361.666
InChiKey
FFFFRWZWCLOBJH-VMPITWQZSA-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

  • 沸点:
    509.6±50.0 °C(predicted)
  • 密度:
    1.46±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.6
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

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:
    (4-溴苄基)三苯基溴化磷鎓5-chloro-2,3-dihydro-1-benzoxepin-4-carboxaldehydesodium ethanolate 作用下, 以 甲苯 为溶剂, 反应 8.25h, 以70%的产率得到4-[2-(4-bromo-phenyl)-vinyl]-5-chloro-2,3-dihydrobenzo[b]oxepine
    参考文献:
    名称:
    Microwave-accelerated Wittig olefination of β-chloroacroleins
    摘要:
    The first microwave assisted Wittig reactions of beta-chloroacroleins with a stabilized ylide are described here. A combination of sodium ethoxide and toluene was found to be optimum and using this reaction condition a number of alkenyl-substituted benzopyran/benzo[b]oxepine/2-chromenone derivatives were prepared within few minutes. The microwave mediated process was found to be comparable with the conventional Wittig reaction in terms of product yields. All the products isolated were found to have E-geometry around the C=C bond. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.12.036
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文献信息

  • Microwave-accelerated Wittig olefination of β-chloroacroleins
    作者:Rabin Bera、G. Dhananjaya、Shambu Nath Singh、Rajender Kumar、K. Mukkanti、Manojit Pal
    DOI:10.1016/j.tet.2008.12.036
    日期:2009.2
    The first microwave assisted Wittig reactions of beta-chloroacroleins with a stabilized ylide are described here. A combination of sodium ethoxide and toluene was found to be optimum and using this reaction condition a number of alkenyl-substituted benzopyran/benzo[b]oxepine/2-chromenone derivatives were prepared within few minutes. The microwave mediated process was found to be comparable with the conventional Wittig reaction in terms of product yields. All the products isolated were found to have E-geometry around the C=C bond. (C) 2008 Elsevier Ltd. All rights reserved.
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