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N,N,4-三甲基苯胺盐酸盐 | 13330-15-9

中文名称
N,N,4-三甲基苯胺盐酸盐
中文别名
苯胺,N,N,4-三甲基-,盐酸
英文名称
N,N,4-trimethylaniline hydrochloride
英文别名
dimethyl-(4-methylphenyl)azanium;chloride
N,N,4-三甲基苯胺盐酸盐化学式
CAS
13330-15-9
化学式
C9H13N*ClH
mdl
——
分子量
171.67
InChiKey
MSWANEMFQROHCW-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):
    2.48
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    3.2
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:63d0d62736a47e615267d6ee2b2989fa
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反应信息

  • 作为反应物:
    描述:
    silver trifluoromethanesulfonateN,N,4-三甲基苯胺盐酸盐二氯甲烷 为溶剂, 以286 mg的产率得到Dimethyl-(4-methylphenyl)azanium;trifluoromethanesulfonate
    参考文献:
    名称:
    Transition Metal‐Free Catalytic C−H Zincation and Alumination
    摘要:

    C−H metalation is the most efficient method to prepare aryl–zinc and –aluminium complexes that are ubiquitous nucleophiles. Virtually all C–H metalation routes to form Al/Zn organometallics require stoichiometric, strong Brønsted bases with no base‐catalyzed reactions reported. Herein we present a catalytic in amine/ammonium salt (Et3N/[(Et3N)H]+) C–H metalation process to form aryl‐zinc and aryl‐aluminium complexes. Key to this approach is coupling an endergonic C–H metalation step with a sufficiently exergonic dehydrocoupling step between the ammonium salt by‐product of C–H metalation ([(Et3N)H]+) and a Zn–H or Al–Me containing complex. This step, forming H2/MeH, makes the overall cycle exergonic while generating more of the reactive metal electrophile. Mechanistic studies supported by DFT calculations revealed metal‐specific dehydrocoupling pathways, with the divergent reactivity due to the different metal valency (which impacts the accessibility of amine‐free cationic metal complexes) and steric environment. Notably, dehydrocoupling in the zinc system proceeds through a ligand‐mediated pathway involving protonation of the b‐diketiminate Cg position. Given this process is applicable to two disparate metals (Zn and Al), other main group metals and ligand sets are expected to be amenable to this transition metal‐free, catalytic C−H metalation.

    DOI:
    10.1002/anie.202404848
  • 作为产物:
    参考文献:
    名称:
    通过(杂)芳基三氟甲磺酸酯的布赫瓦尔德-哈特维希胺化钯催化的N,N-二甲基苯胺的合成。
    摘要:
    这项工作描述了由二甲胺和芳基三氟甲磺酸酯合成N,N-二甲基苯胺衍生物。钯催化的C–N键的形成以极高的产率进行,使用了不复杂的催化体系,温和的碱和三氟甲磺酸酯作为亲电子试剂,可以从便宜的苯酚中轻松获得。N,N-二甲基苯胺是多功能反应伙伴,代表有机合成中有用但未充分利用的结构单元。
    DOI:
    10.1021/acs.joc.0c00491
  • 作为试剂:
    描述:
    参考文献:
    名称:
    Catalytic process for producing alkylene carbonates
    摘要:
    公开号:
    US02773070A1
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文献信息

  • <i>N</i>-Methylation and Trideuteromethylation of Amines via Magnesium-Catalyzed Reduction of Cyclic and Linear Carbamates
    作者:Marc Magre、Marcin Szewczyk、Magnus Rueping
    DOI:10.1021/acs.orglett.0c00988
    日期:2020.4.17
    A new reduction of carbamates to N-methyl amines is presented. The magnesium-catalyzed reduction reaction allows the conversion of cyclic and linear carbamates, including N-Boc protected amines, into the corresponding N-methyl amines and amino alcohols which are of significant interest due to their presence in many biologically active molecules. Furthermore, the reduction can be extended to the formation
    提出了将氨基甲酸酯新还原为N-甲基胺的方法。催化的还原反应使包括N- Boc保护的胺在内的环状和线性氨基甲酸酯转化为相应的N-甲基胺和基醇,由于它们在许多生物活性分子中的存在,它们引起了人们的极大兴趣。此外,该还原可以扩展到N-三苯甲基亚甲基标记的胺的形成。
  • Polyethylene composition and process for producing same
    申请人:TOSOH CORPORATION
    公开号:US20040214953A1
    公开(公告)日:2004-10-28
    A polyethylene composition prepared by polymerizing ethylene and an optional olefin with ≧3 carbon atoms in the presence of a macromonomer, is provided. The macromonomer is a vinyl-terminated ethylene polymer prepared by polymerizing ethylene and an optional olefin with ≧3 carbon atoms, and the macromonomer has (A) Mn≧5,000, and Mw/Mn=2-5. The polyethylene composition comprises (C) branched polyethylene prepared by copolymerizing ethylene, the macromonomer and an optional olefin with ≧3 carbon atoms, and the macromonomer. The polyethylene composition has (D) a density of 0.890-0.980 g/cm 3 , (E) Mw=30,000-10,000,000, (F) Mw/Mn=2-30, (G) a long chain branch frequency of 0.01-3 per 1,000 C atoms, and (H) a shrinking factor (g′ value) of 0.1-0.9 as measured by GPC/intrinsic-viscosity. The polyethylene composition can be finely divided particles having (P) a powder bulk density of 0.15-0.50 g/cm 3 .
    本发明提供了一种聚乙烯组合物,其是通过在存在大分子单体的情况下聚合乙烯和可选的具有≥3个碳原子的烯烃制备的。所述大分子单体是通过聚合乙烯和可选的具有≥3个碳原子的烯烃制备的,其具有(A) Mn≥5,000,且Mw/Mn=2-5的乙烯基端的聚合物。所述聚乙烯组合物包括(C)支化聚乙烯,其是通过共聚乙烯、大分子单体和可选的具有≥3个碳原子的烯烃制备的。所述聚乙烯组合物具有(D)密度为0.890-0.980 g/cm3,(E) Mw=30,000-10,000,000,(F) Mw/Mn=2-30,(G) 0.01-3个每1,000个C原子的长链支化频率,以及(H) 通过GPC/内禀粘度测量的收缩因子(g'值)为0.1-0.9。所述聚乙烯组合物可以是具有(P)粉末堆密度为0.15-0.50 g/cm3的细分散粒子。
  • Method of producing a crosslinked coating in the manufacture of integrated circuits
    申请人:Hessell T. Edward
    公开号:US20050215713A1
    公开(公告)日:2005-09-29
    The present invention is directed to a method of providing a thermally curable coating composition for to provide positive photoresists layers, underlayers for multiple layer resists, antireflective coatings, bottom layer antireflective coatins, dielectric layers, photoresist layers, hard mask etch stops, in the manufacture of integrated circuits. More particularly, the present invention is directed to a method of using a thermally activable latent acid or a thermal acid generator, a N-benzylpyridinium or N-benzylanilinium salt of a strong acid, as a catalyst in a polymerizable composition suitable for preparing such coatings and layers. The present invention is also directed to novel compositions comprising benzylpyridinium and benzylanilinium salts of a strong acid, such as sulfonic acid or disulfonic acid as thermal acid generators.
    本发明涉及一种提供热固性涂层组合物的方法,用于提供正向光刻层、多层光刻底层、抗反射涂层、底层抗反射涂层、介电层、光刻层、硬膜层刻停等,用于集成电路的制造。更具体地,本发明涉及一种使用热活性潜酸或热酸发生剂、强酸的N-苄基吡啶或N-苄基苯胺盐作为催化剂的聚合物组合物的方法,适用于制备这种涂层和层。本发明还涉及一种新型组合物,包括苄基吡啶和苄基苯胺盐,作为热酸发生剂的强酸,如磺酸或二磺酸
  • Transition metal compound, olefin polymerization catalyst comprising the compound, and process for production of olefin polymer
    申请人:Tosoh Corporation
    公开号:EP0786466A1
    公开(公告)日:1997-07-30
    A polyolefin of a high molecular weight is produced by using a catalyst comprising a transition metal compound represented by General Formula (1):
    使用由通式(1)表示的过渡属化合物组成的催化剂生产高分子量聚烯烃:
  • Olefin polymerisation catalysts and processes for producing olefin polymers
    申请人:TOSOH CORPORATION
    公开号:EP0849292A1
    公开(公告)日:1998-06-24
    Catalysts for olefin polymerization which consist essentially of a transition metal compound, a modified clay compound and an organic aluminum compound, wherein the modified clay compound comprises a reaction product of a clay mineral and a proton acid salt of a specific amine compound, as well as a method of polymerizing olefins using such catalysts. It is possible thereby to obtain olefin polymers with high productivity and low ash content.
    烯烃聚合催化剂,主要由过渡属化合物、改性粘土化合物和有机铝化合物组成,其中改性粘土化合物包括粘土矿物和特定胺化合物的质子酸盐的反应产物,以及使用这种催化剂聚合烯烃的方法。由此可以获得生产率高、灰分含量低的烯烃聚合物。
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同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫