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(1S,2R)-1-Bromomethyl-2-(2-bromo-propyl)-cyclohexane | 137303-31-2

中文名称
——
中文别名
——
英文名称
(1S,2R)-1-Bromomethyl-2-(2-bromo-propyl)-cyclohexane
英文别名
——
(1S,2R)-1-Bromomethyl-2-(2-bromo-propyl)-cyclohexane化学式
CAS
137303-31-2
化学式
C10H18Br2
mdl
——
分子量
298.061
InChiKey
LIJGMAVDUMSSBM-VXRWAFEHSA-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

反应信息

  • 作为反应物:
    描述:
    (1S,2R)-1-Bromomethyl-2-(2-bromo-propyl)-cyclohexane 在 potassium sulfide 作用下, 以 乙醇 为溶剂, 生成 (1S,3aS,7aS)-1-Ethyl-octahydro-benzo[c]thiophene 、 (1R,3aS,7aS)-1-Ethyl-octahydro-benzo[c]thiophene 、 trans-3-methyl-trans-2-thiadecalin 、 trans-3-methyl-trans-2-thiadecalin
    参考文献:
    名称:
    Synthesis of 1-substituted trans-2-thiahydrindanes and 3-substituted trans-2-thiadecalins
    摘要:
    Methods of synthesis of 1-R-trans-2-thiahydrindanes and 3-R-trans-2-thiadecalins from trans-1-methoxymethyl-2-chlorocyclohexane have been developed. The order of the chromatographic elution of the isomeric sulfides formed has been found. The configurations of the compounds have been established by H-1 and C-13 NMR spectroscopy. The characteristics of the intermediate and final compounds are given. The splitting of 1-R-trans-2-oxahydrindanes and 3-R-trans-2-oxadecalins by the PBr3/conc. HBr system has been effected.
    DOI:
    10.1007/bf01172271
  • 作为产物:
    描述:
    (4aR,8aS)-3-Methyl-octahydro-isochromene 在 氢溴酸三溴化磷 作用下, 以80%的产率得到(1S,2R)-1-Bromomethyl-2-(2-bromo-propyl)-cyclohexane
    参考文献:
    名称:
    Synthesis of 1-substituted trans-2-thiahydrindanes and 3-substituted trans-2-thiadecalins
    摘要:
    Methods of synthesis of 1-R-trans-2-thiahydrindanes and 3-R-trans-2-thiadecalins from trans-1-methoxymethyl-2-chlorocyclohexane have been developed. The order of the chromatographic elution of the isomeric sulfides formed has been found. The configurations of the compounds have been established by H-1 and C-13 NMR spectroscopy. The characteristics of the intermediate and final compounds are given. The splitting of 1-R-trans-2-oxahydrindanes and 3-R-trans-2-oxadecalins by the PBr3/conc. HBr system has been effected.
    DOI:
    10.1007/bf01172271
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