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2-(benzo[b]thiophen-2-yl)furan | 116849-90-2

中文名称
——
中文别名
——
英文名称
2-(benzo[b]thiophen-2-yl)furan
英文别名
2-(furan-2-yl)benzo[b]thiophene;2-(2-furanyl)benzo[b]thiophene;2-(1-Benzothiophen-2-yl)furan
2-(benzo[b]thiophen-2-yl)furan化学式
CAS
116849-90-2
化学式
C12H8OS
mdl
——
分子量
200.261
InChiKey
KHTBACVGLIOXLO-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

物化性质

  • 沸点:
    338.2±17.0 °C(Predicted)
  • 密度:
    1.243±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    41.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    2-巯基苯甲醇三乙胺 作用下, 以 甲苯乙腈 为溶剂, 反应 7.5h, 生成 2-(benzo[b]thiophen-2-yl)furan
    参考文献:
    名称:
    A Simple Synthesis of 2-Substituted 1-Benzothiophenes and 3- Substituted 2H-1-Benzothiopyrans
    摘要:
    (2-巯基苯)甲基三苯基膦溴化物(2)与酰氯或α-卤酮在碱的存在下反应,分别生成2-取代的1-苯并硫菲4和3-取代的2H-1-苯并硫吡喃6(2H-1-苯并硫烯),产率中等到良好。
    DOI:
    10.1055/s-1988-27501
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文献信息

  • A New Zn/TiCl<sub>4</sub>/LiAlH<sub>4</sub> Mediated Approach to 2-Aryl- or 2-Alkyl-Substituted Benzothiophenes via Intramolecular Cyclization
    作者:Yong-Jin Yoon、Sang-Gyeong Lee、Hyung Jeong、Un Yoon、Sang Jang、Un-Aeh Yoo、Su Kim、Ba Truong、Sung Shin、Okram Singh
    DOI:10.1055/s-2007-980345
    日期:2007.6
    Methyl 2-(substituted benzoylthio)benzoates undergo intramolecular ring cyclizations in the presence of Zn/TiCl 4 /LiAlH 4 to give the corresponding 2-aryl- or alkylsubstituted benzo-thiophenes in good yields.
    2-(取代苯甲酰硫基)苯甲酸甲酯在Zn/TiCl 4 /LiAlH 4 存在下进行分子内环环化,以良好的产率得到相应的2-芳基或烷基取代的苯并噻吩。
  • Copper-Catalyzed Synthesis of Benzo[<i>b</i>]thiophenes and Benzothiazoles Using Thiocarboxylic Acids as a Coupling Partner
    作者:Hui Yu、Meishu Zhang、Yuzhe Li
    DOI:10.1021/jo401353w
    日期:2013.9.6
    copper-catalyzed approach to benzo[b]thiophene and benzothiazole derivatives using thiocarboxylic acids as a sulfur source has been developed. In the presence of CuI and 1,10-phen, and n-Pr3N as the base, (2-iodobenzyl)triphenylphosphonium bromide and (2-iodophenylimino)triphenylphosphorane reacted smoothly with thiocarboxylic acids to give benzo[b]thiophene and benzothiazole derivatives in good yields via
    已经开发出一种有效的铜催化方法,以硫代羧酸作为硫源,用于苯并[ b ]噻吩和苯并噻唑衍生物。在CuI和1,10-phen和n -Pr 3 N为碱的情况下,(2-碘苄基)三苯基溴化and和(2-碘苯基亚氨基)三苯基phosph与硫代羧酸平稳反应,生成苯并[ b ]噻吩和苯并噻唑通过顺序的Ullmann型C–S键耦合和Wittig缩合,可以得到高收率的衍生物。
  • POLYMER CONTAINING FURAN CROSSLINKING GROUP AND USE THEREOF
    申请人:Guangzhou Chinaray Optoelectronic Materials Ltd.
    公开号:EP3560917A1
    公开(公告)日:2019-10-30
    The present disclosure provides a polymer containing a furanyl crosslinkable group and the use thereof in an organic electronic device. A polymer containing a furanyl crosslinkable group is represented by the following general formula (I): wherein x and y each represent a repeating unit, and both x and y are positive integers; formula and formula are each independently selected from the group consisting of an aryl containing 5 - 40 ring atoms and a heteroaryl containing 5-40 ring atoms; formula is a linking group, and formula is selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, aralkyl, and heteroalkyl; and R2, R3 and R4 are each independently selected from the group consisting of H, D, F, CN, alkyl, fluoroalkyl, aryl, heteroaryl, amino, Si, germyl, alkoxy, aryloxy, fluoroalkoxy, siloxane, siloxy, deuterated alkyl, deuterated fluoroalkyl, deuterated aryl, deuterated heteroaryl, deuterated amino, deuterated silyl, deuterated germyl, deuterated alkoxy, deuterated aryloxy, deuterated fluoroalkoxy, deuterated siloxane, and deuterated siloxy.
    本公开提供了一种含有呋喃基交联基团的聚合物及其在有机电子设备中的用途。含有呋喃基可交联基团的聚合物由以下通式(I)表示: 其中 x 和 y 各代表一个重复单元,且 x 和 y 均为正整数; 式中 和式 各自独立地选自含 5-40 个环原子的芳基和含 5-40 个环原子的杂芳基组成的组; 式 是连接基团,而式 选自由烷基、烷氧基、氨基、烯基、炔基、芳基和杂烷基组成的组; R2、R3 和 R4 各自独立地选自由 H、D、F、CN、烷基、氟烷基、芳基、杂芳基、氨基、Si、芽基、烷氧基、芳氧基、氟烷氧基、硅氧烷、硅氧基、氚代烷基、氚代氟烷基、氚代烯基、炔基、芳烷基和杂烷基组成的组、氚代氟烷基、氚代芳基、氚代杂芳基、氚代氨基、氚代硅烷基、氚代胚芽 基、氚代烷氧基、氚代芳氧基、氚代氟烷氧基、氚代硅氧烷和氚代硅氧基。
  • Polymers containing furanyl crosslinkable groups and uses thereof
    申请人:GUANGZHOU CHINARAY OPTOELECTRONIC MATERIALS LTD.
    公开号:US11289654B2
    公开(公告)日:2022-03-29
    The present disclosure provides a polymer represented by the following general formula (I): wherein x and y each represent a repeating unit, and both x and y are positive integers; formula and formula are each independently selected from the group consisting of an aryl containing 5-40 ring atoms and a heteroaryl containing 5-40 ring atoms; formula is a linking group, and formula is selected from the group consisting of alkyl, alkoxy, amino, alkenyl, alkynyl, aralkyl, and heteroalkyl; and R2, R3 and R4 are each independently selected from the group consisting of H, D, F, CN, alkyl, fluoroalkyl, aryl, heteroaryl, amino, Si, germyl, alkoxy, aryloxy, fluoroalkoxy, siloxane, siloxy, deuterated alkyl, deuterated fluoroalkyl, deuterated aryl, deuterated heteroaryl, deuterated amino, deuterated silyl, deuterated germyl, deuterated alkoxy, deuterated aryloxy, deuterated fluoroalkoxy, deuterated siloxane, and deuterated siloxy.
    本公开提供了一种由以下通式 (I) 表示的聚合物: 其中 x 和 y 各代表一个重复单元,且 x 和 y 均为正整数; 式中 和公式 各自独立地选自含 5-40 个环原子的芳基和含 5-40 个环原子的杂芳基组成的 组;式中 是连接基团,式 选自由烷基、烷氧基、氨基、烯基、炔基、芳基和杂烷基组成的组; R2、R3 和 R4 各自独立地选自由 H、D、F、CN、烷基、氟烷基、芳基、杂芳基、氨基、 Si、芽基、烷氧基、芳氧基、氟烷氧基、硅氧烷、硅氧基、氚代烷基、氚代氟烷基、氚代芳基、氚代芳基和杂烷基组成的组、氚代氟烷基、氚代芳基、氚代杂芳基、氚代氨基、氚代硅烷基、氚代胚芽 基、氚代烷氧基、氚代芳氧基、氚代氟烷氧基、氚代硅氧烷和氚代硅氧基。
  • One-Pot Synthesis of Amine-Substituted Aryl Sulfides and Benzo[<i>b</i>]thiophene Derivatives
    作者:Zhongyu Duan、Sadananda Ranjit、Xiaogang Liu
    DOI:10.1021/ol100816g
    日期:2010.5.21
    A series of amine-substituted aryl sulfides have been synthesized from nitroaryl halides via a simple one-pot procedure involving metal-free C S cross-coupling and in situ nitro group reduction. Various nitroaryl halides were reacted with thiols in recyclable poly(ethylene glycol) to afford the amine-substituted aryl sulfides in high yield. Additionally, the cross-coupling reactions of nitro- and aldehyde-substituted aryl halides with benzyl thiols under the same reaction conditions were demonstrated to afford benzothiazole and phenylbenzo[b]thiophene derivatives.
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