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2,2,4,4-tetramethyl-3-(4-acetyl)benzylidene-1,5-dioxa-2,4-disilacycloheptane | 1177254-30-6

中文名称
——
中文别名
——
英文名称
2,2,4,4-tetramethyl-3-(4-acetyl)benzylidene-1,5-dioxa-2,4-disilacycloheptane
英文别名
1-[4-[(2,2,4,4-Tetramethyl-1,5,2,4-dioxadisilepan-3-ylidene)methyl]phenyl]ethanone;1-[4-[(2,2,4,4-tetramethyl-1,5,2,4-dioxadisilepan-3-ylidene)methyl]phenyl]ethanone
2,2,4,4-tetramethyl-3-(4-acetyl)benzylidene-1,5-dioxa-2,4-disilacycloheptane化学式
CAS
1177254-30-6
化学式
C16H24O3Si2
mdl
——
分子量
320.536
InChiKey
NFEIFVBZHQBHCI-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

计算性质

  • 辛醇/水分配系数(LogP):
    3.81
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2,2,4,4-tetramethyl-3-(4-acetyl)benzylidene-1,5-dioxa-2,4-disilacycloheptane(E)-1-(2-iodovinyl)-4-methylbenzene 在 bis(η3-allyl-μ-chloropalladium(II)) 、 四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 以80%的产率得到(E,E)-1-(4-acetylphenyl)-4-(4-methylphenyl)buta-1,3-diene
    参考文献:
    名称:
    Cyclic 1,1-bis(silyl)alkenes—new building blocks for the stereoselective synthesis of unsymmetrical (E)-stilbenes and (E,E)-1,4-diarylbuta-1,3-dienes
    摘要:
    A new efficient synthetic protocol for the highly stereoselective synthesis Of Unsymmetrical (or symmetrical) (E)-stilbenes and (E,E)-1,4-diarylbuta-1,3-dienes based on sequential palladium-catalyzed Heck arylation-Hiyama cross-coupling reactions using cyclic gem-bis(silyl)ethene as alkenyl building block is reported. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.01.113
  • 作为产物:
    描述:
    4-碘代苯乙酮2,2,4,4-tetramethyl-1,5-dioxa-3-methylene-2,4-disilacycloheptane 在 palladium diacetate 、 silver nitrate三乙胺三苯基膦 作用下, 以 乙腈 为溶剂, 反应 1.0h, 以72%的产率得到2,2,4,4-tetramethyl-3-(4-acetyl)benzylidene-1,5-dioxa-2,4-disilacycloheptane
    参考文献:
    名称:
    Cyclic 1,1-bis(silyl)alkenes—new building blocks for the stereoselective synthesis of unsymmetrical (E)-stilbenes and (E,E)-1,4-diarylbuta-1,3-dienes
    摘要:
    A new efficient synthetic protocol for the highly stereoselective synthesis Of Unsymmetrical (or symmetrical) (E)-stilbenes and (E,E)-1,4-diarylbuta-1,3-dienes based on sequential palladium-catalyzed Heck arylation-Hiyama cross-coupling reactions using cyclic gem-bis(silyl)ethene as alkenyl building block is reported. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.01.113
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文献信息

  • Cyclic 1,1-bis(silyl)alkenes—new building blocks for the stereoselective synthesis of unsymmetrical (E)-stilbenes and (E,E)-1,4-diarylbuta-1,3-dienes
    作者:Piotr Pawluć、Grzegorz Hreczycho、Andrzej Suchecki、Maciej Kubicki、Bogdan Marciniec
    DOI:10.1016/j.tet.2009.01.113
    日期:2009.7
    A new efficient synthetic protocol for the highly stereoselective synthesis Of Unsymmetrical (or symmetrical) (E)-stilbenes and (E,E)-1,4-diarylbuta-1,3-dienes based on sequential palladium-catalyzed Heck arylation-Hiyama cross-coupling reactions using cyclic gem-bis(silyl)ethene as alkenyl building block is reported. (C) 2009 Elsevier Ltd. All rights reserved.
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