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5-bromo-1,3-dihydro-N,N,1,1-tetramethyl-6-isobenzofuranamine | 156054-97-6

中文名称
——
中文别名
——
英文名称
5-bromo-1,3-dihydro-N,N,1,1-tetramethyl-6-isobenzofuranamine
英文别名
——
5-bromo-1,3-dihydro-N,N,1,1-tetramethyl-6-isobenzofuranamine化学式
CAS
156054-97-6
化学式
C12H16BrNO
mdl
——
分子量
270.169
InChiKey
ZXAPBEBYRBUDHZ-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

  • 沸点:
    333.1±42.0 °C(predicted)
  • 密度:
    1.336±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

反应信息

  • 作为反应物:
    描述:
    丙酰氯5-bromo-1,3-dihydro-N,N,1,1-tetramethyl-6-isobenzofuranamine正丁基锂 作用下, 生成 1,3-dihydro-1,1-dimethyl-6-dimethylamino-α-ethyl-5-isobenzofuranmethanol
    参考文献:
    名称:
    Synthesis of Isobenzofuran Derivatives as heterocyclic analogues of the herbicidesindone B
    摘要:
    The target compounds 21-27 were synthesized via bromination of the N,N,1,1-tetramethylisobenzofuranamines 13, 15 and 16, subsequent bromine-lithium exchange and reaction with propanal or propanoyl chloride, respectively. In the course of some model reactions undertaken to test a synthetic strategy based on directed ortho-lithiation governed by the dimethylamino-group a useful synthesis of the ketone 3 was developed.
    DOI:
    10.1002/prac.19943360411
  • 作为产物:
    描述:
    1,3-Dihydro-N,N,1,1-tetramethyl-6-isobenzofuranamin 作用下, 以 甲醇 为溶剂, 反应 0.67h, 以85%的产率得到5-bromo-1,3-dihydro-N,N,1,1-tetramethyl-6-isobenzofuranamine
    参考文献:
    名称:
    Synthesis of Isobenzofuran Derivatives as heterocyclic analogues of the herbicidesindone B
    摘要:
    The target compounds 21-27 were synthesized via bromination of the N,N,1,1-tetramethylisobenzofuranamines 13, 15 and 16, subsequent bromine-lithium exchange and reaction with propanal or propanoyl chloride, respectively. In the course of some model reactions undertaken to test a synthetic strategy based on directed ortho-lithiation governed by the dimethylamino-group a useful synthesis of the ketone 3 was developed.
    DOI:
    10.1002/prac.19943360411
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