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2-methoxycarbonyl-1-(but-3'-ynyl)-4-methylenebutyrolactone | 1032192-52-1

中文名称
——
中文别名
——
英文名称
2-methoxycarbonyl-1-(but-3'-ynyl)-4-methylenebutyrolactone
英文别名
Methyl 3-but-3-ynyl-5-methylidene-2-oxooxolane-3-carboxylate
2-methoxycarbonyl-1-(but-3'-ynyl)-4-methylenebutyrolactone化学式
CAS
1032192-52-1
化学式
C11H12O4
mdl
——
分子量
208.214
InChiKey
BCSZILVBHHQTJM-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):
    1.5
  • 重原子数:
    15
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    2-(methoxycarbonyl)-2-(prop-2-ynyl)hex-5-ynoic acid 在 gold (III) oxide 作用下, 以 乙腈 为溶剂, 反应 2.0h, 以80%的产率得到2-methoxycarbonyl-1-(but-3'-ynyl)-4-methylenebutyrolactone
    参考文献:
    名称:
    Au2O3 as a Stable and Efficient Catalyst for the Selective Cycloisomerization of γ-Acetylenic Carboxylic Acids to γ-Alkylidene-γ-Butyrolactones
    摘要:
    展示了市售金氧化物(Au2O3)作为催化剂,在通过一种通用、高效且简便的过程,将带有羧酸的炔烃环化为相应γ-烷叉基-γ-丁内酯中的高潜力。该反应表现出高度化学选择性、区域选择性和立体选择性。5-内型环化和反式金化是Au2O3催化剂的普遍趋势。
    DOI:
    10.1055/s-2008-1032108
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文献信息

  • Au<sub>2</sub>O<sub>3</sub> as a Stable and Efficient Catalyst for the Selective Cycloisomerization of γ-Acetylenic Carboxylic Acids to γ-Alkylidene-γ-Butyrolactones
    作者:Véronique Michelet、Patrick Toullec、Emilie Genin、Sylvain Antoniotti、Jean-Pierre Genêt
    DOI:10.1055/s-2008-1032108
    日期:——
    The high potential of commercially available Au2O3 as a catalyst in the cyclization of alkynes bearing carboxylic acids to the corresponding γ-alkylidene-γ-butyrolactones through a general, efficient and easy procedure is presented. The reaction shows a high degree of chemo-, regio-, and stereoselectivity. The 5-exo mode of cyclization and anti auration are a general trend for the Au2O3 catalyst.
    展示了市售金氧化物(Au2O3)作为催化剂,在通过一种通用、高效且简便的过程,将带有羧酸的炔烃环化为相应γ-烷叉基-γ-丁内酯中的高潜力。该反应表现出高度化学选择性、区域选择性和立体选择性。5-内型环化和反式金化是Au2O3催化剂的普遍趋势。
  • Novel Pd heterogeneous catalysts for cycloisomerisation of acetylenic carboxylic acids
    作者:Florentina Neaţu、Loredana Proteşescu、Mihaela Florea、Vasile I. Pârvulescu、Cristian M. Teodorescu、Nicoleta Apostol、Patrick Y. Toullec、Véronique Michelet
    DOI:10.1039/c0gc00258e
    日期:——
    The Pd-TPPTS complex (TPPTS - trisodium salt of 3,3′,3′′-phosphanetriyl benzenesulfonic acid) and PdCl42− salt heterogenised onto Zn2AlNO3 layered double hydroxide (LDH) using an ion-exchange procedure, have been shown to be efficient green catalysts in the cycloisomerisation reaction of acetylenic carboxylic acids to the corresponding 5-membered heterocycles.
    Pd-TPPTS配合物(TPPTS-三(3,3',3''-膦酸基)苯磺酸三钠盐)和PdCl42−盐通过离子交换程序负载到Zn2AlNO3层状双氢氧化物(LDH)上,已被证明在炔酸的环异构化反应中是高效的绿色催化剂,能够生成相应的5元杂环。
  • INTRAMOLECULAR CYCLIZATION OF γ-ACETYLENIC ACIDS USING DENDRIMER-ENCAPSULATED Pd2+ CATALYSTS
    作者:Kiyotomi Kaneda、Zen Maeno、Tomoo Mizugaki、Koichiro Jitsukawa、Takato Mitsudome
    DOI:10.3987/com-12-s(n)96
    日期:——
    Polyamine dendrimer-encapsulated Pd2+ catalysts were prepared by complexation of PdCl2 with internal tertiary amino groups of the dendrimer. The fifth-generation Pd2+ dendrimer catalyst showed cooperative catalysis between Pd2+ species and the internal nanocavity consisting of regularly arranged tertiary amino groups to promote the intramolecular cyclization of gamma-acetylenic acids efficiently.
  • W(CO)5(L)-Catalyzed Cyclization of α-Alkynyl-β-dicarbonyl Derivatives: Synthesis of Methylenelactones, Furans, and Methylenecyclopentanes
    作者:Sunggak Kim、Xiangjian Meng
    DOI:10.1055/s-0032-1316536
    日期:2012.8
    W(CO)(5)(L)-Catalyzed cyclization of alpha-alkynyl-beta-keto acids, keto esters, and diketones provides methylenelactones, furans, and methylenecyclopentanes via 5-exo-dig cyclization. Also, the present approach can be further applied to 5-endo-dig cyclization.
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