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diethyl {(E)-4-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]but-2-en-1-yl}phosphonate | 1357009-93-8

中文名称
——
中文别名
——
英文名称
diethyl {(E)-4-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]but-2-en-1-yl}phosphonate
英文别名
5-[(E)-4-diethoxyphosphorylbut-2-enyl]sulfonyl-1-phenyltetrazole
diethyl {(E)-4-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]but-2-en-1-yl}phosphonate化学式
CAS
1357009-93-8
化学式
C15H21N4O5PS
mdl
——
分子量
400.395
InChiKey
TWNAMEAZMSGHDB-CMDGGOBGSA-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):
    1.1
  • 重原子数:
    26
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    122
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    diethyl {(E)-4-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]but-2-en-1-yl}phosphonate正己醛双(三甲基硅烷基)氨基钾 作用下, 以 四氢呋喃 为溶剂, 反应 1.41h, 以80%的产率得到diethyl (2E,4E)-deca-2,4-dien-1-ylphosphonate
    参考文献:
    名称:
    Synthesis of Conjugated Polyenes via Sequential Condensation of Sulfonylphosphonates and Aldehydes
    摘要:
    Selective metalation of sulfonylphosphonates results in sufficiently stable carbanions that undergo chemoselective Julia-Kocienski condensation with various aldehydes to provide (E)-allylic phosphonates in good yields and selectivities. The subsequent Horner-Wadsworth-Emmons condensation with aldehydes is used to synthesize various unsymmetrical trans-dienes, trienes, and tetraenes. This methodology is utilized for the concise synthesis of a naturally occurring fluorescent probe for membrane properties, beta-parinaric acid.
    DOI:
    10.1021/ol203431e
  • 作为产物:
    描述:
    diethyl [(E)-4-bromobut-2-en-1-yl]phosphonate1-苯基-5-巯基四氮唑四丁基碘化铵potassium carbonate 、 ammonium molybdate 、 双氧水 作用下, 以 N,N-二甲基甲酰胺乙醇 为溶剂, 反应 24.0h, 以92%的产率得到diethyl {(E)-4-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]but-2-en-1-yl}phosphonate
    参考文献:
    名称:
    Synthesis of Conjugated Polyenes via Sequential Condensation of Sulfonylphosphonates and Aldehydes
    摘要:
    Selective metalation of sulfonylphosphonates results in sufficiently stable carbanions that undergo chemoselective Julia-Kocienski condensation with various aldehydes to provide (E)-allylic phosphonates in good yields and selectivities. The subsequent Horner-Wadsworth-Emmons condensation with aldehydes is used to synthesize various unsymmetrical trans-dienes, trienes, and tetraenes. This methodology is utilized for the concise synthesis of a naturally occurring fluorescent probe for membrane properties, beta-parinaric acid.
    DOI:
    10.1021/ol203431e
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