CAS: 92-94-4; P-Terphenyl

该化合物其结构特征为结构,由三个相连的苯环(C6H5)组成,以线性方式排列;这种芳香烃在室温下是一种无色晶体固体,以其高熔点和在不同条件下的稳定性而著称;p-Terbon在水中是无法溶解的,但在苯和甲苯等有机溶剂中是可溶解的;它具有显著的热稳定性,在高温应用中经常被用作热传输媒介;此外,p-terbon在有机电子领域,特别是在开发荧光材料方面,以及作为闪光时能够释放光的闪烁探测器的一个部件,其化学特性包括能够进行典型的亚罗化合物的电益替代反应,使其在合成有机化学中成为多用途的复合化合物.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

CAS号624-38-4 1,4-二碘苯 | CAS号98-80-6 苯硼酸 | CAS号589-87-7 对溴碘苯 | CAS号106-37-6 对二溴苯 | CAS号106-46-7 1,4-二氯苯 | CAS号92-66-0 4-溴联苯 | CAS号143-66-8 四苯硼钠 | CAS号71-43-2 苯 | CAS号1591-31-7 4-碘联苯 | CAS号2051-62-9 4-氯联苯 | CAS号3073-05-0 对五联苯 | CAS号3365-85-3 4,4''-二氨基三联苯 | CAS号14739-51-6 1-phenyl-4-[3-[... | CAS号4499-83-6 对六联苯 | CAS号2005-10-9 6H-苯并[c]苯并吡喃-6-酮 | CAS号947-84-2 2-苯基苯甲酸 | CAS号84-15-1 邻二苯基苯 | CAS号21711-52-4 1,4-bis(4-chlor... | CAS号65-85-0 苯甲酸 | CAS号92-92-2 4-苯基苯甲酸

合成工艺路线路线简述

  • 合成目标产物 P-Terphenyl 主要起始原料 1-Bromo-4-Iodobenzene And Phenylboronic Acid
  • 21113-62-2 = 92-94-4
    反应条件:1.1 Reagents: Ceric Ammonium Nitrate,Tetrabutylammonium Hydrogen Sulfate Solvents: Chloroform
    标题:Generation Of The 1,4-Diphenylcyclohexane-1,4-Diyl Radical Cation By Cerium(Iv) Catalyzed Denitrogenation Of The Azoalkane 1,4-Diphenyl-2,3-Diazabicyclo[2.2.2]Oct-2-Ene And Its Reluctance To Undergo Cope Rearrangement
    作者:Adam,Waldemar; Grabowski,Sven; Miranda,Miguel A.; Ruebenacker,Martin
    参考文献:Journal Of The Chemical Society 日期:1988 卷标:(2) 页码:142-3]

    98-80-6 + 106-39-8 = 92-94-4
    反应条件:1.1 Reagents: Tripotassium Phosphate Catalysts: Palladium Chloride,N2,N2,N6,N6-Tetrakis[(Diphenylphosphino)Methyl]-2,6-Pyridinediamine Solvents: Dimethylacetamide; 1 H,100 °C1.2 Solvents: O-Xylene; 2 H,90 °C
    标题:N,N,N',N'-Tetra(Diphenylphosphinomethyl)Pyridine-2,6-Diamine/palladium Catalyzed Suzuki-Miyaura Coupling Of Aryl And Heteroaryl Halides
    作者:Guo,Fei-Chen; Zhou,Rong; Jiang,Zhi-Jie; Wang,Wei; Fu,Hai-Yan; Et Al
    参考文献:Catalysis Communications 日期:2015 卷标:66 页码:87-90]

    98-80-6 = 92-94-4
    反应条件:1.1 Reagents: Tripotassium Phosphate Catalysts: (Sp-4-4)-[1,3-Bis[2,6-Bis(1-Methylethyl)Phenyl]-1,3-Dihydro-2H-Imidazol-2-Yliden... Solvents: Ethanol; 6 H,60 °C
    标题:Cyclometalated 2-Phenylimidazole Palladium Carbene Complexes In The Catalytic Suzuki-Miyaura Cross-Coupling Reaction
    作者:Micksch,Maik; Tenne,Mario; Strassner,Thomas
    参考文献:Organometallics 日期:2014 卷标:33(15) 页码:3966-3976]

    98-80-6 + 106-46-7 = 92-94-4
    反应条件:1.1 Reagents: Potassium Carbonate Catalysts: 18-Crown-6,Palladium Trifluoroacetate,2-Dicyclohexylphosphino-2′,6′-Dimethoxybiphenyl Solvents: Carbon Dioxide; 18 H,110 Bar,120 °C
    标题:The Suzuki-Miyaura Cross-Coupling Of Bromo- And Chloroarenes With Arylboronic Acids In Supercritical Carbon Dioxide
    作者:Kuchurov,Ilya V.; Vasil'Ev,Andrei A.; Zlotin,Sergei G.
    参考文献:Mendeleev Communications 日期:2010 卷标:20(3) 页码:140-142]

    98-80-6 + 92-66-0 = 92-94-4
    反应条件:1.1 Catalysts: [1,1′-Binaphthalene]-4,4′-Diamine (Complexes With Palladium Dichloride),Palladium Chloride (Complexes With Naphthidine) Solvents: 1,4-Dioxane; 2 H,Rt1.2 Reagents: Tripotassium Phosphate Solvents: 1,4-Dioxane; 5 Min,Rt1.3 5 H,80 °C
    标题:Naphthidine Di(Radical Cation)S-Stabilized Palladium Nanoparticles For Efficient Catalytic Suzuki-Miyaura Cross-Coupling Reactions
    作者:Desmarets,Christophe; Omar-Amrani,Rafik; Walcarius,Alain; Lambert,Jacques; Champagne,Benoit; Et Al
    参考文献:Tetrahedron 日期:2008 卷标:64(2) 页码:372-381]

    98-80-6 = 92-94-4
    反应条件:1.1 Reagents: Tripotassium Phosphate,Potassium Fluoride Catalysts: Disodium Tetrachloropalladate Solvents: Dimethyl Sulfoxide,Water; 55 H,Rt -> 80 °C; 18 H,80 °C; 80 °C -> Rt
    标题:Homogeneous Catalysts Supported On Soluble Polymers: Biphasic Suzuki-Miyaura Coupling Of Aryl Chlorides Using Phase-Tagged Palladium-Phosphine Catalysts
    作者:An Der Heiden,Markus; Plenio,Herbert
    参考文献:Chemistry - A European Journal 日期:2004 卷标:10(7) 页码:1789-1797]

    98-80-6 + 624-38-4 = 92-94-4
    反应条件:1.1 Reagents: Potassium Carbonate Catalysts: Palladium,Copper Solvents: Dimethylformamide1.2 -
    标题:Copper-Catalyzed Suzuki Cross-Coupling Using Mixed Nanocluster Catalysts
    作者:Thathagar,Mehul B.; Beckers,Jurriaan; Rothenberg,Gadi
    参考文献:Journal Of The American Chemical Society 日期:2002 卷标:124(40) 页码:11858-11859]

    98-80-6 + 624-38-4 = 92-94-4
    反应条件:1.1 Reagents: Potassium Carbonate Catalysts: Chitosan,N-2-Propyn-1-Yl (Propargylated-Chitosan Functionalized Iron Oxide Supported; Post-Treated With Pd(Oac)2) Solvents: Ethanol,Water; 2 H,80 °C
    标题:Triazole Framework: A Strategic Structure For C-H...X Hydrogen Bonding And Practical Design Of An Effective Pd-Catalyst For Carbonylation And Carbon-Carbon Bond Formation
    作者:Mohammadsaleh,Fatemeh; Jahromi,Maryam Dehdashti; Hajipour,Abdol Reza; Hosseini,Seyed Mostafa; Niknam,Khodabakhsh
    参考文献:Rsc Advances 日期:2021 卷标:11(34) 页码:20812-20823]

    98-80-6 + 106-46-7 = 92-94-4
    反应条件:1.1 Reagents: Potassium Hydroxide Catalysts: Palladium Diacetate,2′-(Dicyclohexylphosphino)-N,N-Dimethyl[1,1′-Biphenyl]-2-Amine Solvents: Toluene; 7 - 8 H,90 °C
    标题:Buchwald Ligand-Assisted Suzuki Cross-Coupling Of Polychlorobenzenes
    作者:Vasil'Ev,Andrei A.; Burukin,Alexander S.; Zhdankina,Galina M.; Zlotin,Sergei G.
    参考文献:Mendeleev Communications 日期:2021 卷标:31(3) 页码:400-402]

    98-80-6 + 106-37-6 = 92-94-4
    反应条件:1.1 Reagents: Potassium Carbonate Catalysts: Palladium,Silica,N4-[3-(Triethoxysilyl)Propyl]-2,4,6-Pyrimidinetriamine (Palladium Complexes) Solvents: Ethanol,Water; 15 Min,100 °C
    标题:The Synthesis Of Sba-Pr-3Ap@pd And Its Application As A Highly Dynamic,Eco-Friendly Heterogeneous Catalyst For Suzuki-Miyaura Cross-Coupling Reaction
    作者:Mohajer,Fatemeh; Mohammadi Ziarani,Ghodsi; Badiei,Alireza
    参考文献:Research On Chemical Intermediates 日期:2020 卷标:46(11) 页码:4909-4922]

    591-50-4 + 5122-94-1 = 92-94-4
    反应条件:1.1 Reagents: Potassium Carbonate Catalysts: Palladium Solvents: Ethanol; 10 Min; 3 Min,80 °C1.2 Solvents: Ethanol; 30 Min,80 °C
    标题:Minimalization Of Metallic Pd Formation In Suzuki Reaction With A Solid-State Organometallic Catalyst
    作者:Li,Bowen; Zeng,Hua Chun
    参考文献:Acs Applied Materials & Interfaces 日期:2020 卷标:12(30) 页码:33827-33837]

    98-80-6 + 106-37-6 = 92-94-4
    反应条件:1.1 Reagents: Tripotassium Phosphate Catalysts: Palladium Solvents: Ethanol,Water; 6 H,80 °C
    标题:Spatially Isolated Palladium In Porous Organic Polymers By Direct Knitting For Versatile Organic Transformations
    作者:Wang,Xinbo; Min,Shixiong; Das,Swapan K.; Fan,Wei; Huang,Kuo-Wei; Et Al
    参考文献:Journal Of Catalysis 日期:2017 卷标:355 页码:101-109]

    591-50-4 + 5122-94-1 = 92-94-4
    反应条件:1.1 Reagents: Potassium Carbonate Catalysts: Palladium,Graphene Solvents: Dimethylformamide,Water; 6 Min,90 °C
    标题:3D Graphene/nylon Rope As A Skeleton For Noble Metal Nanocatalysts For Highly Efficient Heterogeneous Continuous-Flow Reactions
    作者:Zhang,Sai; Shen,Xuetao; Zheng,Zhiping; Ma,Yuanyuan; Qu,Yongquan
    参考文献:Journal Of Materials Chemistry A: Materials For Energy And Sustainability 日期:2015 卷标:3(19) 页码:10504-10511]

    98-80-6 + 106-37-6 = 92-94-4
    反应条件:1.1 Reagents: Potassium Carbonate Catalysts: (Sp-4-3)-[2,6-Bis[(Di-1-Piperidinylphosphino-Kp)Amino]Phenyl-Kc]Chloropalladium Solvents: 1-Butanol,1,4-Dioxane,Water; 25 °C; 0.5 H,25 °C -> 100 °C1.2 Reagents: Water; 100 °C; 100 °C -> Rt
    标题:The 1,3-Diaminobenzene-Derived Aminophosphine Palladium Pincer Complex {c6H3[nhp(Piperidinyl)2]2Pd(Cl)} - A Highly Active Suzuki-Miyaura Catalyst With Excellent Functional Group Tolerance
    作者:Bolliger,Jeanne L.; Frech,Christian M.
    参考文献:Advanced Synthesis & Catalysis 日期:2010 卷标:352(6) 页码:1075-1080]

    591-50-4 + 99770-93-1 = 92-94-4
    反应条件:1.1 Reagents: Silver Carbonate Catalysts: Tetrakis(Triphenylphosphine)Palladium Solvents: Tetrahydrofuran
    标题:Efficient Synthesis Of Substituted Terphenyls By Suzuki Coupling Reaction
    作者:Chaumeil,Helene; Le Drian,Claude; Defoin,Albert
    参考文献:Synthesis 日期:2002 卷标:(6) 页码:757-760]

    98-80-6 + 92-66-0 = 92-94-4
    反应条件:1.1 Reagents: Tetrabutylammonium Bromide,Tripotassium Phosphate Catalysts: Palladium Diacetate Solvents: Dimethylformamide
    标题:Pdcl2(Set2)2 And Pd(Oac)2: Simple And Efficient Catalyst Precursors For The Suzuki Cross-Coupling Reaction
    作者:Zim,Danilo; Monteiro,Adriano L.; Dupont,Jairton
    参考文献:Tetrahedron Letters 日期:2000 卷标:41(43) 页码:8199-8202]

    98-80-6 + 92-66-0 = 92-94-4
    反应条件:1.1 Reagents: Tripotassium Phosphate Solvents: Ethanol,Water; 1 H,Rt
    标题:Palladium-Anchored N-Heterocyclic Carbenes In A Porous Organic Polymer: A Heterogeneous Composite Catalyst For Eco-Friendly C-C Coupling
    作者:Let,Sumanta; Dam,Gourab K.; Samanta,Partha; Fajal,Sahel; Dutta,Subhajit; Et Al
    参考文献:Journal Of Organic Chemistry 日期:2022 卷标:87(24) 页码:16655-16664]

    98-80-6 + 589-87-7 = 92-94-4
    反应条件:1.1 Reagents: Potassium Hydroxide Catalysts: 2721440-87-3 Solvents: Methanol; 3 H,Reflux
    标题:Synthesis Of Tetranuclear Complex Of Pd(Ii) With Thiosemicarbazone Ligands Derived From 2-Quinolone And Its Catalytic Evaluation In Suzuki-Miyaura-Type Coupling Reactions And Alkoxylation Of Chloroquinolines
    作者:Nandhini,Sundar; Dharani,Sivadasan; Elamathi,Chennakrishnan; Dallemer,Frederic; Prabhakaran,Rathinasabapathi
    参考文献:Applied Organometallic Chemistry 日期:2021 卷标:35(12)]

    98-80-6 + 92-66-0 = 92-94-4
    反应条件:1.1 Reagents: Potassium Tert-Butoxide Catalysts: [9-(Amino-Kn)-2,3,5,6,14,15-Hexafluoro-9,10-Dihydro-9,10[1′,2′]-Benzenoanthracen... Solvents: Isopropanol; 2 H,80 °C
    标题:Triptycene Ring Metal Palladium Compound And Use Thereof
    参考文献:China]

    324-74-3 = 92-94-4
    反应条件:1.1 Catalysts: Palladium Diacetate,2′-(Dicyclohexylphosphino)-N,N-Dimethyl[1,1′-Biphenyl]-2-Amine Solvents: Tetrahydrofuran; Rt; 16 H,80 °C
    标题:Aryl Fluoride Activation Through Palladium-Magnesium Bimetallic Cooperation: A Mechanistic And Computational Study
    作者:Wu,Chen; Mccollom,Samuel P.; Zheng,Zhipeng; Zhang,Jiadi; Sha,Sheng-Chun; Et Al
    参考文献:Acs Catalysis 日期:2020 卷标:10(14) 页码:7934-7944
(1R)-Trans-1,2-Dichloro-Cyclohexane置于selenium,三氯化铝体系中,化学反应生成 对三联苯
参考文献:Nenitzescu; Curcaneanu,Chemische Berichte,1937,Vol. 70,P. 346,348
标题:Nenitzescu; Curcaneanu,Chemische Berichte,1937,Vol. 70,P. 346,348

海关参考信息

专利信息


专利号:US-7652164-B2
优先权日:2005-09-13
标题:Process for the direct synthesis of trialkoxysilane
发明人:LEWIS KENRICK M; MEREIGH ABELLARD T; O'YOUNG CHI-LIN; CAMERON RUDOLPH A
权利人:MOMENTIVE PERFORMANCE MAT INC
摘要:The Direct Synthesis of trialkoxysilane is carried out by conducting the Direct Synthesis reaction of silicon and alcohol, optionally in solvent, in the presence of a catalytically effective amount of Direct Synthesis catalyst and an effective catalyst-promoting amount of Direct Synthesis catalyst promoter, said promoter being an organic or inorganic compound possessing at least one phosphorus-oxygen bond.

专利号:US-7429672-B2
优先权日:2006-06-09
标题 :Process for the direct synthesis of trialkoxysilane
发明人:LEWIS KENRICK M; CAMERON RUDOLPH A; RITSCHER LEGAL REPRESENTATIVE KAREN
权利人:MOMENTIVE PERFORMANCE MAT INC
摘要:This invention discloses a process to improve reaction stability in the Direct Synthesis of trialkoxysilanes. The process is particularly effective in the Direct Synthesis of triethoxysilane and its higher alkyl cognates providing improved triethoxysilane yields.

专利号:US-2025197202-A1
优先权日:2023-12-15
标题 :Synthesis of new polymers for the manufacture of solid hydrogen transfer agents
发明人:GÓMEZ EMILIO LEAL; MANCERA LEÓN PABLO TORRES; JUÃ?REZ JORGE ANCHEYTA; MARTÃ?NEZ FERNANDO ALONSO; VÃ?ZQUEZ LAURA OLIVIA ALEMÃ?N
权利人:MEXICANO INST PETROL
摘要:This disclosure refers to a method for the synthesis of polymers with weight average molecular weights greater than 50,000 g/mol, chemically inert, with a minimum decomposition temperature of 425° C., and a main chain composed only of carbon-carbon bonds, which contain structures of the type of naphthalene, phenanthrene, anthracene, pyrene, carbazole or any other where two or more aromatic rings of six carbon atoms of the benzene-type are fused, which may or may not contain aromatic heterocycles. In addition, the polymers obtained from the present disclosure may or may not contain fluorine atoms in their structure. The synthesis described here is carried out by means of polycondensation between a polycyclic aromatic compound and a compound with a carbonyl group in its structure in a strong acid medium.

专利号:US-6512081-B1
优先权日:1997-07-21
标题:Synthesis of dithioester chain transfer agents and use of bis(thioacyl) disulfides or dithioesters as chain transfer agents
发明人:RIZZARDO ENZIO; THANG SAN HOA; MOAD GRAEME
权利人:E I DUPONT NEMOURS AND COMPANY; COMMW SCIENT IND RES ORG
摘要:This invention relates to the synthesis of dithiocarboxylic acid esters by reaction of bis(thioacyl) disulphides, thioacetals or vinylidane bis(thioether) with free-radicals (optionally in the presence of monomers). The invention also relates to processes for the synthesis of polymers utilising these dithioesters as polymerisation regulators (chain transfer agents) or to the use of bis(thioacyl) disulphides to generate dithioester chain transfer agents in situ.

专利号:US-RE39650-E
优先权日:1996-10-10
标 题:Surface-active additives in the direct synthesis of trialkoxysilanes
发明人:MENDICINO FRANK D; LEWIS KENRICK M; MAGRI SEBASTIANO; YU HUA; CHILDRESS THOMAS E
权利人:GEN ELECTRIC
摘要:Disclosed is a process in which surface-active additives are used in the slurry phase Direct Synthesis of trialkoxysilanes to shorten the period between the start of the reaction and the attainment of steady-state rates and selectivities, to improve product yields and to control or prevent foam formation. Compositions comprising silicone antifoam compounds and fluorosilicone polymers are the preferred surface-active additives of the instant process.

专利号:US-7148356-B2
优先权日:2001-07-13
标题:Process for the catalytic synthesis of biaryls and polymers from aryl compounds
发明人:SMITH III MILTON R; MALECZKA ROBERT E
权利人:UNIV MICHIGAN STATE
摘要:A process for producing organic substituted aromatic or heteroaromatic compounds including biaryl and biheteroaryl compounds in a two-step reaction. In the first step, the aromatic or heteroaromatic compound is borylated in a reaction comprising a borane or diborane reagent (any boron reagent where the boron reagent contains a B—H, B—B or B—Si bond) and an iridium or rhodium catalytic complex. In the second step, a metal catalyst catalyzes the formation of the organic substituted aromatic or heteroaromatic compound from the borylated compound and an electrophile such as an aryl or organic halide, triflate (OSO 2 CF 3 ), or nonaflate (OSO 2 C 4 F 9 ). The steps in the process can be performed in a single reaction vessel or in separate reaction vessels. The present invention also provides a process for synthesis of complex polyphenylenes starting from halogenated aromatic compounds.
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合成参考文献


参考文献:10.1063/1.2110155
摘要:Trofymluk O, Levchenko AA, Navrotsky A. Interfacial effects on vitrification of confined glass-forming liquids. J Chem Phys. 2005 Nov 15;123(19):194509. doi: 10.1063/1.2110155.
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