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3-(prop-1-yn-1-yl)furan

中文名称
——
中文别名
——
英文名称
3-(prop-1-yn-1-yl)furan
英文别名
3-Prop-1-ynylfuran;3-prop-1-ynylfuran
3-(prop-1-yn-1-yl)furan化学式
CAS
——
化学式
C7H6O
mdl
——
分子量
106.124
InChiKey
STXLENZCMKFJQR-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):
    1.7
  • 重原子数:
    8
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    13.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    3-(prop-1-yn-1-yl)furan1,3-二碘-5,5-二甲基海因triethylamine tris(hydrogen fluoride) 作用下, 以 二氯甲烷 为溶剂, 反应 16.0h, 以26%的产率得到(E)-3-(1-fluoro-2-iodoprop-1-en-1-yl)furan
    参考文献:
    名称:
    用基于DIH和HF的试剂控制炔烃的单和双碘氟化
    摘要:
    公开了使用1,3-二碘-5,5,-二甲基乙内酰脲和基于HF的试剂进行内部和末端炔的区域和立体选择性碘氟化的新方案。该方法用于从市售原料中分两步制备氟化他莫昔芬衍生物。还提出了一种可控制末端炔烃的区域选择性双碘氟化的简便方法。
    DOI:
    10.1021/acs.orglett.8b00321
  • 作为产物:
    描述:
    3-溴呋喃2-丁炔酸 在 bis-triphenylphosphine-palladium(II) chloride 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯1,4-双(二苯基膦)丁烷 作用下, 以 二甲基亚砜 为溶剂, 反应 12.0h, 以33%的产率得到3-(prop-1-yn-1-yl)furan
    参考文献:
    名称:
    用基于DIH和HF的试剂控制炔烃的单和双碘氟化
    摘要:
    公开了使用1,3-二碘-5,5,-二甲基乙内酰脲和基于HF的试剂进行内部和末端炔的区域和立体选择性碘氟化的新方案。该方法用于从市售原料中分两步制备氟化他莫昔芬衍生物。还提出了一种可控制末端炔烃的区域选择性双碘氟化的简便方法。
    DOI:
    10.1021/acs.orglett.8b00321
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文献信息

  • CHAIN MULTIYNE COMPOUND, PREPARATION METHOD AND APPLICATION THEREOF
    申请人:Xiamen University
    公开号:US20180065908A1
    公开(公告)日:2018-03-08
    The present invention relates to fields of organic chemistry and organometallic chemistry. The present invention discloses a chain multiyne compound, a preparation method thereof and an application in synthesizing a fused-ring metallacyclic compound. A structure of the chain multiyne compound in the present invention is shown as Formula I below. The present invention also provides a preparation method of the chain multiyne compound and an application thereof in a synthesis of a fused-ring metallacyclic compound. The chain multiyne compound disclosed in the present invention has multiple functional groups and the structure of the chain multiyne compound is adjustable. The chain multiyne compound can also be used to synthesize the fused-ring metallacyclic compound efficiently. The preparation method of the chain multiyne compound disclosed in the present invention is simple, which can be used to prepare the chain multiyne compound rapidly and efficiently.
    本发明涉及有机化学和有机化学领域。本发明公开了一种链状多炔化合物,其制备方法及在合成融环属环化合物中的应用。本发明中的链状多炔化合物的结构如下式I所示。本发明还提供了链状多炔化合物的制备方法及其在合成融环属环化合物中的应用。本发明公开的链状多炔化合物具有多个功能基团,其结构可调整。链状多炔化合物还可用于高效合成融环属环化合物。本发明公开的链状多炔化合物的制备方法简单,可用于快速高效地制备链状多炔化合物。
  • Samarium(II) Monoalkyl Complex Supported by a β‐Diketiminato‐Based Tetradentate Ligand: Synthesis, Structure, and Catalytic Hydrosilylation of Internal Alkynes
    作者:Xiaojuan Liu、Qingqing Wen、Li Xiang、Xuebing Leng、Yaofeng Chen
    DOI:10.1002/chem.202000342
    日期:2020.4.24
    The synthesis and catalytic applications of trivalent rare-earth metal alkyl complexes have been well developed, but the chemistry of divalent rare-earth metal alkyl complexes lagged much behind. Herein, we report the synthesis, structure, and catalytic applications of a samarium(II) monoalkyl complex supported by a β-diketiminato-based tetradentate ligand, [LSmCH(SiMe3 )2 ] (L=[MeC(NDipp)CHC(Me)NCH2
    三价稀土属烷基络合物的合成和催化应用已得到很好的发展,但二价稀土属烷基络合物的化学反应却落后很多。在这里,我们报告的合成,结构和催化的applications(II)单烷基络合物的支持基于β-二酮氨基甲酸的四齿配体[LSmCH(SiMe3)2](L = [MeC(NDipp)CHC(Me) NCH 2 CH 2 N(Me)CH 2 CH 2 NMe 2]-,Dipp = 2,6-(iPr)2 C 6 H 3)。该复合物是通过化sa [LSm(μ-I)] 2和KCH(SiMe3)2的盐复分解反应合成的,产率为63%。其结构的特征在于单晶X射线衍射,显示出扭曲的方字塔配位几何形状。
  • Rhodium-Catalyzed Regioselective Synthesis of N-Secondary Alkyl Indoles via Intermolecular Cyclization of N-Nitrosoanilines and Unsymmetrical Alkynes
    作者:Yi Dong、Heng Xu、Yiting Chang、Tingting Hou
    DOI:10.1055/s-0041-1738453
    日期:2023.12
    A Cp*Rh-catalyzed C–H functionalization/cyclization to afford 2,3-substituted N-secondary alkyl indole derivatives is described. This intermolecular cyclization of N-secondary nitrosoanilines and unsymmetrically substituted alkynes has good performances in yields, substrate scope, and regioselectivities.
    描述了Cp*Rh 催化的 C–H 官能化/环化以提供 2,3-取代的N-仲烷基吲哚生物。N-仲亚硝基苯胺和不对称取代的炔烃的分子间环化在产率、底物范围和区域选择性方面具有良好的性能。
  • Chain multiyne compound, preparation method and application thereof
    申请人:Xiamen University
    公开号:US10287225B2
    公开(公告)日:2019-05-14
    The present invention relates to fields of organic chemistry and organometallic chemistry. The present invention discloses a chain multiyne compound, a preparation method thereof and an application in synthesizing a fused-ring metallacyclic compound. A structure of the chain multiyne compound in the present invention is shown as Formula I below. The present invention also provides a preparation method of the chain multiyne compound and an application thereof in a synthesis of a fused-ring metallacyclic compound. The chain multiyne compound disclosed in the present invention has multiple functional groups and the structure of the chain multiyne compound is adjustable. The chain multiyne compound can also be used to synthesize the fused-ring metallacyclic compound efficiently. The preparation method of the chain multiyne compound disclosed in the present invention is simple, which can be used to prepare the chain multiyne compound rapidly and efficiently.
    本发明涉及有机化学和有机化学领域。本发明公开了一种链状多炔化合物、其制备方法以及在合成熔环茂属化合物中的应用。本发明中链多炔化合物的结构如下式 I 所示。本发明还提供了链式多炔化合物的制备方法及其在合成熔环茂属环化合物中的应用。本发明公开的链式多炔化合物具有多个官能团,且链式多炔化合物的结构可调。该链多炔化合物还可用于高效合成熔环茂属环化合物。本发明公开的链式多炔化合物的制备方法简单,可用于快速高效地制备链式多炔化合物。
  • REMEDIES OR PREVENTIVES FOR URINARY INCONTINENCE AND MORPHINAN DERIVATIVES HAVING NITROGEN-CONTAINING HETEROCYCLIC GROUP
    申请人:TORAY INDUSTRIES, INC.
    公开号:EP1555266B1
    公开(公告)日:2014-05-21
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