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ethyl (2-furan-2-yl)butyrate

中文名称
——
中文别名
——
英文名称
ethyl (2-furan-2-yl)butyrate
英文别名
Ethyl 2-(furan-2-yl)butanoate
ethyl (2-furan-2-yl)butyrate化学式
CAS
——
化学式
C10H14O3
mdl
——
分子量
182.219
InChiKey
MWEKRZUASVMSHC-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):
    2.1
  • 重原子数:
    13
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    39.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

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文献信息

  • Efficient synthesis of functionalized furans and benzofurans based on a ‘[3+2] cyclization/oxidation’ strategy
    作者:Esen Bellur、Ilia Freifeld、Peter Langer
    DOI:10.1016/j.tetlet.2005.02.040
    日期:2005.3
    Functionalized furans and benzofurans were prepared by DDQ oxidation of 2-alkylidenetetrahydrofurans, which are readily available by one-pot cyclizations of 1,3-dicarbonyl dianions or 1,3-bis-silyl enol ethers.
    通过2-亚烷基四氢呋喃的DDQ氧化制备官能化的呋喃和苯并呋喃,这可以通过一锅式环合1,3-二羰基二价阴离子或1,3-双-甲硅烷基烯醇醚而容易获得。
  • Efficient Synthesis of Furan-2-ylacetates, 7-(Alkoxycarbonyl)benzofurans, and 7-(Alkoxycarbonyl)-2,3-dihydrobenzofurans Based on Cyclization Reactions of Free and Masked Dianions:  A “Cyclization/Dehydrogenation” Strategy
    作者:Esen Bellur、Peter Langer
    DOI:10.1021/jo051767i
    日期:2005.11.1
    A variety of furan-2-ylacetates have been prepared by dehydrogenation of monocyclic 2-alkylidene-tetrahydrofurans, which are readily available by cyclizations of open-chained 1,3-dicarbonyl dianions with 1-bromo-2-chloroethane. 5'H-[2,3']Bifuranyl-2'-ones are available based on sequential "cyclization/dehydrogenation" reactions of alpha-acetyl-gamma-butyrolactones. A variety of 7-(alkoxycarbonyl)-benzofarans and 7-(alkoxycarbonyl)-2,3-dihydrobenzofurans were prepared by a cyclization/ dehydrogenation strategy. These reactions rely on cyclizations of 2-oxocycloalkane-1-carboxylate/derived 1,3-dicarbonyl dianions ("free dianions") or 1,3-bis-silyl enol ethers ("masked dianions") with various 1,2-dielectrophiles.
  • Synthesis of Functionalized Furans Based on a ‘[3+2] Cyclization/Bromination­/Elimination’ Strategy
    作者:Peter Langer、Esen Bellur
    DOI:10.1055/s-2006-926301
    日期:——
    The bromination of 2-alkylidenetetrahydrofurans -readily available via one-pot [3+2] cyclizations - afforded 2-alkylidene-3-bromotetrahydrofurans. Elimination of hydrogen bromide and subsequent aromatization of these compounds provided a convenient approach to functionalized furans.
    2-亚烷基四氢呋喃的溴化-通过一锅[3+2]环化很容易获得-得到2-亚烷基-3-溴四氢呋喃。溴化氢的消除和这些化合物的随后芳构化为官能化呋喃提供了一种方便的方法。
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