CAS: 628-21-7; 1,4-Diiodobutane

该化合物是一种卤代烷,其特点是位于丁烷链终端碳中的两个碘原子,该化合物主要用作有机合成的多用途构件,特别是在准备异环,聚合物和交叉反应时;其在核生殖替代和消化反应中的高度反应性能,对于建造更长的碳链或循环结构很有价值;碘原子提供了极好的离子组特性,促进了高效的授电或循环过程;1,4-二碘丁烷还被用于材料科学,用于合成导电聚合物和液晶;妥善处理由于其光敏度和潜在毒性而必不可少.

结构式图片

相似化合物

628-77-3 629-09-4 10297-05-9

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合成工艺路线路线简述

    1,4-丁二醇 反应生成 1,4-二碘代丁烷
    参考文献:二碘四磷(p 2 I 4)是一种从醇类区域选择性合成碘代烷烃的有价值的试剂
    标题:二碘四磷(p 2 I 4)是一种从醇类区域选择性合成碘代烷烃的有价值的试剂
    摘要:P 2 I 4在cs 2中和20oc时,伯,仲和叔醇区域选择性地转化,并以高收率的烷基碘化物转化.
    DOI:10.1016/s0040-4039(01)86222-5

    专利信息


    专利号:US-10364220-B2
    优先权日:2012-12-21
    标题:Synthesis of succinimides and quaternary ammonium ions for use in making molecular sieves
    发明人:SCHMITT KIRK D; ZUSHMA STEPHEN; BURTON ALLEN W
    权利人:EXXONMOBIL CHEMICAL PATENTS INC
    摘要:The present invention relates to the synthesis of succinimides, in particular to a method for the synthesis of a succinimide compound, comprising the step of reacting an alkyne, with carbon monoxide and ammonia or an amine, in the presence of an iron catalyst, wherein the reaction is carried out in an amine liquid phase and/or in the absence of an ether solvent. The succinimides may be reduced to quaternary ammonium cations which may be used as structure directing agents in the synthesis of molecular sieves.

    专利号:WO-2024260325-A1
    优先权日:2023-06-19
    标题 :Synthesis of macrocyclic compound and medical use of macrocyclic compound
    发明人:LU HONGFU; DING XIAO; REN FENG
    权利人:INSILICO MEDICINE IP LTD
    摘要:Provided in the present invention are the synthesis of a macrocyclic compound and the medical use of the macrocyclic compound. Specifically, provided in the present invention are a compound as show in formula (II), a stereoisomer thereof or a pharmaceutically acceptable salt thereof, which can be used as a CDK7 inhibitor.

    专利号:US-7557099-B2
    优先权日:2004-03-01
    标题 :Pyrrolobenzodiazepines as key intermediates in the synthesis of dimeric cytotoxic pyrrolobenzodiazepines
    发明人:HOWARD PHILIP WILSON; KANG GYOUNG-DONG
    权利人:SPIROGEN LTD
    摘要:Compounds and a method of synthesis of compounds of formula (Ia) or (Ib): and salts, solvates, and chemically protected forms thereof, wherein the dotted lines indicate the optional presence of a double bond between C1 and C2 or C2 and C3; R 2 and R 3 are independently selected from —H, â•?O, â•?CH 2 , —CN, —R, OR, halo, â•?CH—R, O—SO 2 —R, CO 2 R and COR; R 10 is a carbamate-based nitrogen protecting group; and R 11 is an oxygen protecting group.

    专利号:US-9005573-B2
    优先权日:2011-12-22
    标 题:Layered conversion synthesis of zeolites
    发明人:NICHOLAS CHRISTOPHER P; MILLER MARK A
    权利人:UOP LLC
    摘要:A new synthesis technique has been developed to prepare a family of coherently grown composites of at least two zeotypes. Examples of these composites are represented by the empirical formula.n nNa n M m k+ T t Al 1-x E x Si y O z n nwhere “nâ€? is the mole ratio of Na to (Al+E), M represents at least one metal of zinc, Group 1, Group 2, Group 3 and the lanthanide series of the periodic table, and any combination thereof, “mâ€? is the mole ratio of M to (Al+E), “kâ€? is the average charge of the metal or metals M, T is the organic structure directing agent or agents, “tâ€? is the mole ratio of N from the organic structure directing agent or agents to (Al+E), and E is a framework element such as gallium. The synthesis technique is the Layered Conversion Synthesis technique.

    专利号:US-2024199658-A1
    优先权日:2022-12-01
    标 题:Direct synthesis of organotin alkoxides
    发明人:JILEK ROBERT E; REED CHRISTOPHER J; NOVAS BRYAN
    权利人:INPRIA CORP
    摘要:Synthesis techniques are described for forming organotin trialkoxide compounds via direct alkylation of tin alkoxides. A first method involves reacting an alkali metal tin trialkoxide with an organohalide compound (RXn, where X is a halide atom and n≥1) to form a monoorgano tin trialkoxide represented by the formula R[Sn(OR′)3]n. The method can be used to form polytin trialkoxide compounds with a plurality of radiation sensitive C—Sn bonds. R and R′ include organo groups and can optionally comprise hetero-atoms and/or unsaturated bonds. A second method involves the ultraviolet light-driven reaction of a di-tin tetraalkoxide with an organohalide compound (RX) to form a monoorgano trialkoxide represented by the formula RSn(OR′)3. A third method involves the visible or ultraviolet light-driven reaction of a di-tin tetraalkoxide or an alkali metal tin trialkoxide with an fluorinated organohalide compound (RFX) to form a fluorinated monoorgano trialkoxide represented by the formula RFSn(OR′)3. The disclosed methods provide for high mono-organo specificity. Corresponding organotin trialkoxide compositions are also described. The compositions are useful for radiation patterning, especially with EUV radiation. The organotin trialkoxide compositions may be formed as radiation-patternable coatings on substrates.

    专利号:US-2024287269-A1
    优先权日:2021-11-02
    标 题 :Synthesis of poly(phenylene) compound intergrated with functionalized fluorene portion for ion exchange ionomer and ion exchange ionomer
    发明人:ZHANG QIUYING; BAHAR BAMDAD; CHEN MENGJIE
    权利人:USA FORTESCUE IP INC
    摘要:An ion exchange polymer has an ionomer structure containing poly(phenylene) compound integrated with functionalized poly(fluorene). The ion conducting co-polymer includes a poly(fluorene) compound and a poly(phenylene) compound covalently bonded together. The poly(fluorene) compound has a 9H-fluorene structure that is a polycyclic aromatic hydrocarbon having a center ring with five carbon atoms, and a benzene ring on each of opposing sides of said center ring. The poly(phenylene) compound is covalently bonded to each of the pair of benzene rings of the poly(fluorene) compound. A pair of sidechains extends from the center ring of the poly(fluorene) compound to a respective terminal group. The terminal groups are configured on sidechains of the poly(fluorene) compound and can be converted into functional groups such as quaternary ammonium or n-methyl piperidine functional groups. The ion exchange polymer may include a porous scaffold support.
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    📌 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:Total Synthesis Of (−)-Sarain A
    作者:Michael H. Becker,Peter Chua,Robert Downham,Christopher J. Douglas,Neil K. Garg,Sheldon Hiebert,Stefan Jaroch,Richard T. Matsuoka,Joy A. Middleton,Fay W. Ng,Larry E. Overman |发布日期:2007.10.1
    摘要:Studies Toward The Complex Marine Alkaloid Sarain A. Various Strategies Were Conceived, Setbacks Encountered, And Solutions Developed, Ultimately Leading To A Successful Enantioselective Total Synthesis. Our Route To (+)-Sarain A Features A Number Of Key Steps, Including An Asymmetric Michael Addition To Install The C4'-C3'-C7' Stereotriad, An Enoxysilane-N-Sulfonyliminium Ion Cyclization To Set The C3 Quaternary

    合成参考文献


    摘要:Chang, C.-S.; Wu, Y.-T., Science of Synthesis, (2010) 45, 968.
    摘要:Nahm Garrett, M.; Johnson, J. S., Science of Synthesis Knowledge Updates, (2012) 2, 27.
    摘要:Witt, D., Science of Synthesis Knowledge Updates, (2019) 2, 269.
    摘要:Huynh, H. V.; Yuan, D., Science of Synthesis: N-Heterocyclic Carbenes in Catalytic Organic Synthesis, (2016) 1, 29.
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