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2-溴-5-(三甲基硅烷基)噻吩 | 18246-28-1

中文名称
2-溴-5-(三甲基硅烷基)噻吩
中文别名
——
英文名称
2-bromo-5-trimethylsilylthiophene
英文别名
(5-bromothiophen-2-yl)trimethylsilane;2-Bromo-5-(trimethylsilyl)thiophene;(5-bromothiophen-2-yl)-trimethylsilane
2-溴-5-(三甲基硅烷基)噻吩化学式
CAS
18246-28-1
化学式
C7H11BrSSi
mdl
——
分子量
235.22
InChiKey
IXLYRDOGOXBECE-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:
    70°C/2mmHg(lit.)
  • 最大波长(λmax):
    260nm(lit.)

计算性质

  • 辛醇/水分配系数(LogP):
    3.06
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    28.2
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:b163535b1c589a95b483d9ae510ff3f1
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-溴-5-(三甲基硅烷基)噻吩sodium methylate 作用下, 以 甲醇 为溶剂, 生成 2-溴噻吩
    参考文献:
    名称:
    取代的2-噻吩基三甲基硅烷的碱解速率。从头开始计算单取代噻吩的酸度
    摘要:
    Rates of cleavage in NaOMe-MeOH at 50°C have been determined for the mono-substituted 2-trimethylsilylthiophens X·C4H2S·SiMe3-2 with X = H, 3-NO2, 3-Br, 4-Br-, and 5-NO2, -CN, -COPh, -Me, -OMe and -NMe2, and for one disubstituted compound, 4,5-Br2-C4HS-SiMe3-2. For several compounds the rate and product isotope effects have also been determined. The energies involved in the process X·C4H3S → X·C4H2S−
    DOI:
    10.1016/s0022-328x(00)84581-7
  • 作为产物:
    参考文献:
    名称:
    The Analogy between Aromatic Bromination and the Cleavage of Trialkylarylsilanes by Bromine
    摘要:
    DOI:
    10.1021/ja01634a014
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文献信息

  • [EN] COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING (ACYL MOIETIES)<br/>[FR] COMPOSÉS HÉTÉROARYLÉS COUPLÉS PAR UN RÉARRANGEMENT D'HÉTÉROAROMATIQUES HALOGÉNÉS SUIVI PAR UN COUPLAGE OXYDANT (FRACTIONS ACYLE)
    申请人:GEORGIA TECH RES INST
    公开号:WO2013023106A1
    公开(公告)日:2013-02-14
    The inventions disclosed and described herein relate to new and efficient generic methods for making a wide variety of compounds having HAr - Z - Har tricyclic cores, wherein HAr is an optionally substituted five or six membered heteroaryl ring, and Hal is a halogen, and Z is a bridging radical, such as S, Se, NR5, C(O), C(O)C(O), Si(R5)2, SO, SO2, PR5, BR5, C(R5)2 or P(O)R5 and both HAr are covalently bound to one another. The synthetic methods employ a "Base-Catalyzed Halogen Dance" reaction to prepare a metallated compound comprising a five or six membered heteroaryl ring comprising a halogen atom, and then oxidatively coupling the reactive intermediate compound. The compounds of Formula (II) and/or oligomer or polymers comprising repeat units having Formula (II) can be useful for making semi-conducting materials, and/or electronic devices comprising those materials. Acyl compounds can be prepared. Heteroarylene substituents can be used. The tricyclic core can be coupled to itself. The Z group also can be strong electron-withdrawing groups such as C=C(CN)2 or [C=C(CN)2]2. Organic electronic devices can be made including field-effect transistors.
    本公开的和描述的发明涉及制备具有HAr-Z-Har三环核的各种化合物的新型高效通用方法,其中HAr是可选择地取代的五元或六元杂环芳基环,Hal是卤素,Z是桥联基团,如S、Se、NR5、C(O)、C(O)C(O)、Si(R5)2、SO、SO2、PR5、BR5、C(R5)2或P(O)R5,且两个HAr均以共价键结合在一起。合成方法利用“碱催化卤素舞蹈”反应制备包含卤素原子的五元或六元杂环芳基环的金属化合物,然后氧化偶联反应中间体化合物。具有式(II)的化合物和/或包含具有式(II)重复单元的寡聚物或聚合物可用于制备半导体材料和/或包含该材料的电子器件。可以制备酰基化合物。可以使用杂芳基取代基。三环核可以与自身偶联。Z基也可以是强电子吸引基团,如C=C(CN)2或[C=C(CN)2]2。可以制备包括场效应晶体管在内的有机电子器件。
  • Deprotonative C–H Silylation of Functionalized Arenes and Heteroarenes Using Trifluoromethyltrialkylsilane with Fluoride
    作者:Midori Sasaki、Yoshinori Kondo
    DOI:10.1021/ol503671b
    日期:2015.2.20
    A highly selective C–H silylation reaction of functionalized arenes and heteroarenes was developed using Ruppert–Prakash reagent (TMSCF3) activated by alkali metal fluoride. TMSCF3 is considered to play dual roles as a precursor of a mild base and also as a silicon electrophile. The silylation is compatible with sensitive functional groups such as halogen and nitro groups.
    使用被碱金属氟化物活化的Ruppert-Prakash试剂(TMSCF 3),开发了功能化芳烃和杂芳烃的高选择性C-H甲硅烷基化反应。TMSCF 3被认为是温和碱的前体以及亲电子体具有双重作用。甲硅烷基化与敏感的官能团如卤素和硝基相容。
  • [EN] COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING (HETEROARYLENE SPACER MOIETY)<br/>[FR] COMPOSÉS HÉTÉROARYLÉS COUPLÉS PAR UN RÉARRANGEMENT D'HÉTÉROAROMATIQUES HALOGÉNÉS SUIVI PAR UN COUPLAGE OXYDANT (FRACTION ESPACEUR HÉTÉROARYLÈNE)
    申请人:GEORGIA TECH RES INST
    公开号:WO2013023108A1
    公开(公告)日:2013-02-14
    The inventions disclosed and described herein relate to new and efficient generic methods for making a wide variety of compounds having HAr - Z - Har tricyclic cores, wherein HAr is an optionally substituted five or six membered heteroaryl ring, and Hal is a halogen, and Z is a bridging radical, such as S, Sc, NR5, C(O), C(O)C(O), Si(R5)2, SO, S02, PR5, BR5, C(R5)2 or P(O)Rs and both HAr are covalently bound to one another. The synthetic methods employ a "Base-Catalyzed Halogen Dance" reaction to prepare a metallated compound comprising a five or six membered heteroaryl ring comprising a halogen atom, and then oxidatively coupling the reactive intermediate compound. The compounds of Formula (II) and/or oligomer or polymers comprising repeat units having Formula (II) can be useful for making semi-conducting materials, and/or electronic devices comprising those materials. Acyl compounds can be prepared. Heteroarylene substituents can be used. The core tricyclic core can be coupled to itself. The Z group also can be strong electron-withdrawing groups such as C=C(CN)2 or [C=C(CN)212. Organic electronic devices can be made including field-effect transistors. Formula (II).
    本公开的发明涉及一种用于制备具有HAr-Z-Har三环核的各种化合物的新型高效通用方法,其中HAr是可选择地取代的五元或六元杂环芳基环,Hal是卤素,Z是桥联基团,例如S、Sc、NR5、C(O)、C(O)C(O)、Si(R5)2、SO、SO2、PR5、BR5、C(R5)2或P(O)Rs,两个HAr均以共价键结合在一起。合成方法利用“碱催化卤素舞蹈”反应制备包含卤素原子的五元或六元杂环芳基环的金属化合物,然后氧化偶联反应中间体化合物。具有Formula (II)的化合物和/或包含具有Formula (II)重复单元的寡聚物或聚合物可用于制备半导体材料和/或包含该材料的电子器件。可以制备酰基化合物。可以使用杂芳基取代基。核心三环核可以与自身偶联。Z基团也可以是强电子吸引基团,如C=C(CN)2或[C=C(CN)2]2。可以制备包括场效应晶体管在内的有机电子器件。Formula (II)。
  • [EN] COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING (COUPLED TRICYCLIC CORE COMPOUNDS)<br/>[FR] COMPOSÉS HÉTÉROARYLÉS COUPLÉS PAR L'INTERMÉDIAIRE D'UN RÉARRANGEMENT D'HÉTÉROAROMATIQUES HALOGÉNÉS SUIVI PAR UN COUPLAGE OXYDANT (COMPOSÉS À COEURS TRICYCLIQUES COUPLÉS)
    申请人:GEORGIA TECH RES INST
    公开号:WO2013023109A1
    公开(公告)日:2013-02-14
    The inventions disclosed and described herein relate to new and efficient generic methods for making a wide variety of compounds having HAr - Z - Har tricyclic cores (II) from intermediates (I), wherein HAr is an optionally substituted five or six membered heteroaryl ring, and Hal is a halogen, and Z is a bridging radical, such as S, Sc, NRS, C(O), C(O)C(O), Si(R5)2, SO, S02, PRS, BRS, C(R5)2 or P(O)R5 and both HAr are covalently bound to one another. The synthetic methods employ a "Base-Catalyzed Halogen Dance" reaction to prepare a metallated compound comprising a five or six membered heteroaryl ring comprising a halogen atom, and then oxidatively coupling the reactive intermediate compound. The compounds of Formula (II) and/or oligomer or polymers comprising repeat units having Formula (IT) can be useful for making semi-conducting materials, and/or electronic devices comprising those materials. Acyl compounds can be prepared. Heteroary- lene substituents can be used. The core tricyclic core can be coupled to itself. The Z group also can be strong electron-withdrawing groups such as C=C(CN)2 or [C=C(CN)2]2. Organic electronic devices can be made including field-effect transistors. (Formula I, II)
    本文所披露和描述的发明涉及一种新的高效通用方法,用于制备具有HAr-Z-Har三环核(II)的各种化合物,其来源于中间体(I),其中HAr是一个可选择取代的五元或六元杂环芳烃环,Hal是卤素,Z是桥接基团,如S、Sc、NRS、C(O)、C(O)C(O)、Si(R5)2、SO、S02、PRS、BRS、C(R5)2或P(O)R5,两个HAr均以共价键结合在一起。合成方法采用“碱催化卤素舞蹈”反应来制备包含卤素原子的五元或六元杂环芳烃环的金属化合物,然后氧化偶联反应中间体化合物。具有公式(II)的化合物和/或包含具有公式(IT)重复单元的寡聚物或聚合物可用于制备半导体材料,和/或包含这些材料的电子器件。可以制备酰基化合物。可以使用杂芳基取代基。核心三环核可以与自身偶联。Z基团也可以是强电子吸引基团,如C=C(CN)2或[C=C(CN)2]2。可以制造包括场效应晶体管在内的有机电子器件。(公式I,II)
  • [EN] COUPLED HETEROARYL COMPOUNDS VIA REARRANGEMENT OF HALOGENATED HETEROAROMATICS FOLLOWED BY OXIDATIVE COUPLING (ELECTRON WITHDRAWING GROUPS)<br/>[FR] COMPOSÉS HÉTÉROARYLÉS COUPLÉS PAR UN RÉARRANGEMENT D'HÉTÉROAROMATIQUES HALOGÉNÉS SUIVI PAR UN COUPLAGE OXYDANT (GROUPES ÉLECTROATTRACTEURS)
    申请人:GEORGIA TECH RES INST
    公开号:WO2013023107A1
    公开(公告)日:2013-02-14
    The inventions disclosed and described herein relate to new and efficient generic methods for making a wide variety of compounds having HAr - Z - Har tricyclic cores, wherein HAr is an optionally substituted five or six membered heteroaryl ring, and Hal is a halogen, and Z is a bridging radical, such as S, Sc, NR5, C(O), C(O)C(O), Si(R5)2, SO, SO2, PR5, BR5, C(R5)2 or P(O)R5 and both HAr are covalently bound to one another. The synthetic methods employ a "Base-Catalyzed Halogen Dance" reaction to prepare a metallated compound comprising a five or six membered heteroaryl ring comprising a halogen atom, and then oxidatively coupling the reactive intermediate compound. The compounds of Formula (II) and/or oligomer or polymers comprising repeat units having Formula (II) can be useful for making semi-conducting materials, and/or electronic devices comprising those materials. Acyl compounds can be prepared. Heteroarylene substituents can be used. The core tricyclic core can be coupled to itself. The Z group also can be strong electron-withdrawing groups such as C=C(CN)2 or [C=C(CN)2]2. Organic electronic devices can be made including field-effect transistors. Formula (II).
    本公开的发明涉及一种新的高效通用方法,用于制备具有HAr-Z-Har三环核的各种化合物,其中HAr是可选择地取代的五元或六元杂环芳基环,Hal是卤素,Z是桥联基团,如S、Sc、NR5、C(O)、C(O)C(O)、Si(R5)2、SO、SO2、PR5、BR5、C(R5)2或P(O)R5,且两个HAr均以共价键结合在一起。合成方法利用“碱催化卤素舞蹈”反应制备包含卤素原子的五元或六元杂环芳基环的金属化合物,然后氧化偶联反应中间体化合物。具有Formula (II)的化合物和/或包含具有Formula (II)重复单元的寡聚体或聚合物可用于制备半导体材料和/或包含该材料的电子器件。可以制备酰基化合物。可以使用杂芳基取代基。核心三环核可以与自身偶联。Z基团还可以是强电子吸引基团,如C=C(CN)2或[C=C(CN)2]2。可以制备包括场效应晶体管在内的有机电子器件。Formula (II)。
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同类化合物

阿罗洛尔 阿替卡因 阿克兰酯 锡烷,(5-己基-2-噻吩基)三甲基- 邻氨基噻吩(2盐酸) 辛基5-(1,3-二氧戊环-2-基)-2-噻吩羧酸酯 辛基4,6-二溴噻吩并[3,4-b]噻吩-2-羧酸酯 辛基2-甲基异巴豆酸酯 血管紧张素IIAT2受体激动剂 葡聚糖凝胶LH-20 苯螨噻 苯并[c]噻吩-1-羧酸,5-溴-4,5,6,7-四氢-3-(甲硫基)-4-羰基-,乙基酯 苯并[b]噻吩-2-胺 苯并[b]噻吩-2-胺 苯基-[5-(4,4,5,5-四甲基-[1,3,2]二氧杂硼烷-2-基)-噻吩-2-基亚甲基]-胺 苯基-(5-氯噻吩-2-基)甲醇 苯乙酸,-α--[(1-羰基-2-丙烯-1-基)氨基]- 苯乙酰胺,3,5-二氨基-a-羟基-2,4,6-三碘- 苯乙脒,2,6-二氯-a-羟基- 腈氨噻唑 聚(3-丁基噻吩-2,5-二基),REGIOREGULAR 硝呋肼 硅烷,(3-己基-2,5-噻吩二基)二[三甲基- 硅噻菌胺 盐酸阿罗洛尔 盐酸阿罗洛尔 盐酸多佐胺 甲酮,[5-(1-环己烯-1-基)-4-(2-噻嗯基)-1H-吡咯-3-基]-2-噻嗯基- 甲基5-甲酰基-4-甲基-2-噻吩羧酸酯 甲基5-乙氧基-3-羟基-2-噻吩羧酸酯 甲基5-乙基-3-肼基-2-噻吩羧酸酯 甲基5-(氯甲酰基)-2-噻吩羧酸酯 甲基5-(氯乙酰基)-2-噻吩羧酸酯 甲基5-(氨基甲基)噻吩-2-羧酸酯 甲基5-(4-甲氧基苯基)-2-噻吩羧酸酯 甲基5-(4-甲基苯基)-2-噻吩羧酸酯 甲基5-(1,3-二氧戊环-2-基)-2-噻吩羧酸酯 甲基4-硝基-2-噻吩羧酸酯 甲基4-氰基-5-(4,6-二氨基吡啶-2-基)偶氮-3-甲基噻吩-2-羧酸酯 甲基4-氨基-5-(甲硫基)-2-噻吩羧酸酯 甲基4-{[(2E)-2-(4-氰基苯亚甲基)肼基]磺酰}噻吩-3-羧酸酯 甲基4-(氯甲酰基)-3-噻吩羧酸酯 甲基4-(氨基磺酰基氨基)-3-噻吩羧酸酯 甲基3-甲酰氨基-4-甲基-2-噻吩羧酸酯 甲基3-氨基-5-异丙基-2-噻吩羧酸酯 甲基3-氨基-5-(4-溴苯基)-2-噻吩羧酸酯 甲基3-氨基-4-苯基-5-(三氟甲基)-2-噻吩羧酸酯 甲基3-氨基-4-氰基-5-甲基-2-噻吩羧酸酯 甲基3-氨基-4-丙基-2-噻吩羧酸酯 甲基3-[[(4-甲氧基苯基)亚甲基氨基]氨基磺酰基]噻吩-2-羧酸酯