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prenyl 1-propenyl ether | 287195-16-8

中文名称
——
中文别名
——
英文名称
prenyl 1-propenyl ether
英文别名
3-methyl-2-butenyl (E)-1-propenyl ether;3-methyl-1-[(E)-prop-1-enoxy]but-2-ene
prenyl 1-propenyl ether化学式
CAS
287195-16-8
化学式
C8H14O
mdl
——
分子量
126.199
InChiKey
NVDPJMBTLDLZLK-GQCTYLIASA-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):
    2.6
  • 重原子数:
    9
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 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

  • 作为反应物:
    描述:
    prenyl 1-propenyl ether 反应 5.0h, 以51%的产率得到2,3,3-trimethyl-4-pentenal
    参考文献:
    名称:
    Stereoselective Isomerization of Unsymmetrical Diallyl Ethers to Allyl (E)-Vinyl Ethers by a Cationic Iridium Catalyst
    摘要:
    The stereoselective isomerization of unsymmetrical diallyl ethers to allyl (E)-vinyl ethers was carried out in the presence of a cationic iridium(I) catalyst. The catalyst prepared in situ by treating [Ir(cod)(PPh2Me)(2)]PF6 with hydrogen was found to be an excellent catalyst to selectively isomerize the less substituted allyl group to an (E)-vinyl ether.
    DOI:
    10.1080/00397910008086880
  • 作为产物:
    描述:
    1-(2-propenoxy)-3-methyl-2-butene 在 [Ir(THF)2H2(PPh2Me)2]PF6 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 以65%的产率得到prenyl 1-propenyl ether
    参考文献:
    名称:
    Stereoselective Isomerization of Unsymmetrical Diallyl Ethers to Allyl (E)-Vinyl Ethers by a Cationic Iridium Catalyst
    摘要:
    The stereoselective isomerization of unsymmetrical diallyl ethers to allyl (E)-vinyl ethers was carried out in the presence of a cationic iridium(I) catalyst. The catalyst prepared in situ by treating [Ir(cod)(PPh2Me)(2)]PF6 with hydrogen was found to be an excellent catalyst to selectively isomerize the less substituted allyl group to an (E)-vinyl ether.
    DOI:
    10.1080/00397910008086880
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文献信息

  • Encapsulated molecular catalysts in polysiloxane gels: ruthenium cluster-catalyzed isomerization of alkenes
    作者:Yukihiro Motoyama、Motonori Abe、Kazuyuki Kamo、Yusuke Kosako、Hideo Nagashima
    DOI:10.1039/b809937e
    日期:——
    gels are prepared by treatment of polymethylhydrosiloxane with diols in the presence of (mu(3),eta(2),eta(3),eta(5)-acenaphthylene)Ru(3)(CO)(7), and act as reusable catalysts in the isomerization of alkenes without leakage of the catalyst species.
    通过在(mu(3),eta(2),eta(3),eta(5)-))Ru(3)(CO)(7)存在下用二醇处理聚甲基氢硅氧烷来制备新型钌包裹聚硅氧烷凝胶),并在烯烃的异构化中用作可重复使用的催化剂,而不会泄漏催化剂种类。
  • Stereoselective Isomerization of Unsymmetrical Diallyl Ethers to Allyl (<i>E</i>)-Vinyl Ethers by a Cationic Iridium Catalyst
    作者:Yasunori Yamamoto、Ryou Fujikawa、Norio Miyaura
    DOI:10.1080/00397910008086880
    日期:2000.7
    The stereoselective isomerization of unsymmetrical diallyl ethers to allyl (E)-vinyl ethers was carried out in the presence of a cationic iridium(I) catalyst. The catalyst prepared in situ by treating [Ir(cod)(PPh2Me)(2)]PF6 with hydrogen was found to be an excellent catalyst to selectively isomerize the less substituted allyl group to an (E)-vinyl ether.
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