CAS: 17376-04-4; (2-Iodoethyl)Benzene

该化合物是一种有机碘化合物,以2-iodo乙基组替代苯环,这种结构使其成为有机合成中有价值的中间体,特别是在交叉反应和核生殖替代方面,在这种替代中,碘乙基碱作为进一步功能化的被动处理器.在标准条件下,其稳定性允许方便处理和储存,而其再活性可以精确修改复杂的分子结构.该化合物通常用于制药和农用化学研究,以构建碳-碳和碳-乙基联结.其明确界定的化学特性确保合成应用中的再生性,使它成为先进的化学合成的可靠选择.

结构式图片

上下游产品

CAS号622-24-2 β-氯代苯乙烷 | CAS号103-63-9 β-溴苯乙烷 | CAS号60-12-8 苯乙醇 | CAS号292638-84-7 phenylene-ethylene | CAS号458-87-7 2-fluoroethylbenzene | CAS号81609-30-5 2-phenylethylte... | CAS号1229444-43-2 4-(diphenylphos... | CAS号101-97-3 苯乙酸乙酯 | CAS号1229444-44-3 1-甲基-1-[4-(二苯基膦... | CAS号54673-12-0 (1R)-1-acetoxy-... | CAS号1077-11-8 trimethyl(2-phe... | CAS号110683-92-6 (2-fluoro-2-nit... | CAS号108011-20-7 3-(2-phenylethy... | CAS号4410-99-5 2-苯乙硫醇 | CAS号3558-60-9 甲基苯乙基醚 | CAS号5463-92-3 2-乙酰氨基-2-苯乙基丙二醇二乙酯 | CAS号6125-24-2 Β-硝基苯乙烷 | CAS号14171-89-2 6-苯基己-2-酮 | CAS号103-25-3 3-苯丙酸甲酯 | CAS号104-53-0 3-苯丙醛

合成工艺路线路线简述

    📜苯乙酸乙酯置于indium(III) Bromide,1,1,3,3-四甲基二硅氧烷,碘体系中,用 氯仿 用作溶剂,化学反应 1.0H,以92%的收率获得2-碘代乙基苯
    参考文献:铟(III)催化的羧酸的还原溴化和碘化反应,生成烷基溴化物和碘化物:范围,机理和一锅法转变为卤代烷和胺衍生物
    标题:铟(III)催化的羧酸的还原溴化和碘化反应,生成烷基溴化物和碘化物:范围,机理和一锅法转变为卤代烷和胺衍生物
    摘要:描述了高效的铟(III)催化的各种羧酸与1,1,3,3-四甲基二硅氧烷(tmds)和溴或碘源的还原溴化或碘化.该官能团互变对几种官能团具有高耐受性,例如卤素,羟基,硝基,烯烃部分和硫化物部分.该铟催化体系也适用于醛化,酰氯和酯的还原碘化.此外,该还原体系可通过添加亲核试剂用于一锅法合成卤代烷和胺衍生物.通过1 H和13 C NMR监测实验的时间过程以及相应的逐步反应,可以深入了解反应机理.
    Doi:10.1021/jo401529J

    海关参考信息

    专利信息


    专利号:WO-2009115333-A1
    优先权日:2008-03-20
    标 题:Novel synthesis of praziquantel
    发明人:DOEMLING ALEXANDER
    权利人:DOEMLING ALEXANDER
    摘要:The present invention discloses a novel and efficient synthesis of praziquantel (I).

    专利号:WO-2017082924-A1
    优先权日:2015-11-13
    标题 :Peptide and peptide mimetic binding antagonists of polo-like kinase 1 polo box domain and methods of use
    发明人:BURKE TERRENCE R JR; HYMEL DAVID
    权利人:THE US SECRETARY DEPT OF HEALTH & HUMAN SERVICES
    摘要:The description provides novel compounds that may serve as anticancer therapeutics. The compounds of the description bind to polo-like kinases through the polo-box domain. The peptide derivatives of the description have achieved improved efficacy in biochemical assays against Plk1. The description also provides methods of use, methods of preparation, compositions, and kits thereof. Further, the description provides a novel method of design and/or synthesis of phosphoryl-derived peptide derivatives useful as therapeutic agents.

    专利号:US-2023357286-A1
    优先权日:2020-07-24
    标 题:Ketone synthesis and applications
    发明人:KISHI YOSHITO; UMEHARA ATSUSHI
    权利人:HARVARD COLLEGE
    摘要:Provided are new nickel./zirconium-mediated coupling reactions useful in the synthesis of ketone-containing compounds, e.g., halichondrin natural products and related molecules. A feature of the present disclosure is the use of a nickel(I) catalyst in tandem with a nickel (II) catalyst in the Ni/Zr-mediated coupling reactions. Without wishing to be bound by any particular theory, the nickel (I) catalyst selectively activates the electrophilic coupling partner (i.e., the compound of Formula (A)), and the nickel(ll) catalyst selectively activates the nucleophilic coupling partner (i.e., a thioester of Formula (B)). This dual catalyst system leads to improved coupling efficiency and eliminates the need for a large excess of one of the coupling partners (i.e., a compound of Formula (A) or (B)).

    专利号:US-4033949-A
    优先权日:1976-04-14
    标 题:Analogs of thromboxane B2 and processes for their synthesis
    发明人:KELLY ROBERT C; NELSON NORMAN A
    权利人:UPJOHN CO
    摘要:The present specification provides novel intermediates and novel processes for the synthesis of various side chain and skeletal analogs of Thromboxane B 2 (11β-homo-11a-oxa-PGF 2 .sub.α). These analogs are particularly and especially useful as reproductive cycle control agents.

    专利号:US-2008183007-A1
    优先权日:2004-10-08
    标 题 :Process For the Preparation of Alkyl Phosphinic Acids
    发明人:THELIN MATS
    权利人:ASTRAZENECA AB
    摘要:The present invention relates to a new process for the synthesis of alkyl phosphinic acids, and more particularly to a coupling reaction between an alkylhalide and a hypophosphorous acid derivative by a radical initiated reaction. The invention also relates to compounds obtainable by the method of the invention.

    专利号:US-2015158020-A1
    优先权日:2013-12-11
    标题:Synthesis of zeolites using an organoammonium compound
    发明人:NICHOLAS CHRISTOPHER P; MILLER MARK A
    权利人:UOP LLC
    摘要:A method for synthesizing a zeolite includes the steps of: (a) preparing an aqueous mixture comprising water, a substituted hydrocarbon and an amine; (b) reacting the aqueous mixture; (c) obtaining a solution comprising an organoammonium product; (d) forming a reaction mixture including reactive sources of M, Al, Si, optionally seeds of a layered material L, and the solution, wherein M is a metal; and (e) heating the reaction mixture to form the zeolite. The substituted hydrocarbon can be an α,ω-dihalogen substituted alkane, and the amine is preferably essentially incapable of undergoing pyramidal inversion.

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    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Organocerium Additions To Proline-Derived Hydrazones: Synthesis Of Enantiomerically Enriched Amines
    作者:Scott E. Denmark,James P. Edwards,Theodor Weber,David W. Piotrowski |发布日期:2010.5
    摘要:The Addition Of Organocerium Reagents (From Both Organolithium And Organomagnesium Precursors) To Chiral Aldehyde Hydrazones Prepared From 1-Aminoproline Derivatives Has Been Studied. The Additions Proceed In Good Yield And High Diastereoselectivity And With Good Nucleophile (Me, N-Bu, I-Pr, T-Bu, Ph, Etc.) And Substrate Scope (Alkyl, Alkenyl And Aryl). The Resulting Hydrazines Can Be Converted To

    合成参考文献


    摘要:Li, Y.; Xie, W.; Jiang, X., Science of Synthesis Knowledge Updates, (2016) 2, 27.
    摘要:Alonso, D. A.; Nájera, C., Science of Synthesis, (2010) 47, 468.
    摘要:Chciuk, T. V.; Flowers, R. A.; Flowers, R. A., Science of Synthesis Knowledge Updates, (2016) 2, 196.
    摘要:Schatz, J.; Seler, M., Science of Synthesis Knowledge Updates, (2011) 2, 394.
    摘要:Ishii, A., Science of Synthesis Knowledge Updates, (2016) 2, 374.
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