CAS: 599-70-2; (Ethylsulfonyl)Benzene

该化合物是一种有机化合物,其特征是附于苯环的磺酰集团,其乙基集团与硫磺原子相连,其分子结构具有磺酰体功能集团(Eurosulfonyl),该物质集团有助于其化学反应和溶性.该化合物一般是一种无色的黄色液体或固体,视温度和纯度而定.该化合物以其相对高的沸点和有机溶剂中的中度溶性而著称,它可用于各种化学用途,包括有机合成中的试剂和药品的生产.该物质集团的存在增强了其极性,使其得以参与核分裂替代反应.安全数据表明,应当谨慎处理,因为它在与皮肤或眼睛接触时可能会引起刺激.建议在远离不相容物质的寒冷,干的地方适当储存,以保持其稳定性.

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CAS号5535-48-8 苯基乙烯基砜 | CAS号622-38-8 苯乙硫醚 | CAS号963-15-5 顺-1,2-二(苯砜)乙烯 | CAS号5324-64-1 Benzene,[(2-phe... | CAS号122-52-1 亚磷酸三乙酯 | CAS号75-03-6 碘乙烷 | CAS号98-09-9 苯磺酰氯 | CAS号93-54-9 1-苯基-1-丙醇 | CAS号1829-40-9 六苯基二硅氧烷 | CAS号791-31-1 三苯基硅醇 | CAS号622-38-8 苯乙硫醚 | CAS号3112-88-7 苄基苯基砜 | CAS号1589-60-2 1-苯基环己醇 | CAS号1940-18-7 1-乙基环己醇 | CAS号1733-57-9 乙基二苯基氧化膦 | CAS号187527-25-9 (5S)-5,7-Bis-{[...

合成工艺路线路线简述

    丁基硫基苯置于双氧水体系中,用 乙腈 作为反应溶剂,化学反应 1.0H,以34%的收率获得产物乙基苯基砜
    参考文献:Selective Oxidation Of Sulfides And Hydrocarbons With H$_{2}$o$_{2}$ Over Manganese Catalyst Supported On Nanoparticles
    标题:Selective Oxidation Of Sulfides And Hydrocarbons With H$_{2}$o$_{2}$ Over Manganese Catalyst Supported On Nanoparticles
    摘要:一种新的磁性可分离催化剂被制备,该催化剂由二核mn(II)络合物[mn₂(Hl)₂(H₂o)₄]组成,其中hl = 2-[(2-羟基苄叉)-氨基]-3-(4-羟基苯基)-丙酸,支持在功能化的(3-氯丙基)-三甲氧基硅烷(Cptms)涂层磁性纳米颗粒(Mnps)上.合成的催化剂通过多种物理化学和光谱方法进行了表征.结果表明,该固定化复合物在使用过氧化氢(H₂o₂)作为氧化剂的情况下,对不同的硫化物和烃的氧化反应表现出非常好的异相催化活性.催化剂可以通过简单的磁分离方法轻易回收,并且可以重复使用多次,而催化活性几乎没有显著损失.
    DOI:10.3906/kim-1307-50

    海关参考信息

    专利信息


    专利号:US-10253153-B2
    优先权日:2015-04-24
    标题 :Linker and support for solid phase synthesis of nucleic acid, and production method of nucleic acid using said support
    发明人:MAETA ERI; MORI KENJIRO; HORIE SHOHEI; ITO TAKAHIKO; SAITO SHOICHIRO; NAGAO RYUHEI
    权利人:NITTO DENKO CORP
    摘要:The present invention provides a linker for solid phase synthesis of nucleic acid, which consists of a compound represented by the formula (I) or the formula (II), a support for solid phase synthesis of nucleic acid, which has a structure represented by the formula (III), and a production method of a nucleic acid, which uses the support: n nwherein each symbol is as defined in the SPECIFICATION.

    专利号:US-11542269-B2
    优先权日:2018-01-03
    标 题:Prins reaction and compounds useful in the synthesis of halichondrin macrolides and analogs thereof
    发明人:CHOI HYEONG-WOOK; FANG FRANCIS G
    权利人:EISAI R&D MAN CO LTD
    摘要:The invention provides methods utilizing Prins reaction in the preparation of compounds that may be useful as intermediates in the synthesis of halichondrin macrolides and analogs thereof. The invention also provides compounds that may be useful as intermediates in the synthesis of a halichondrin macrolides and methods for preparing the same.

    专利号:US-10913749-B2
    优先权日:2015-05-07
    标 题 :Macrocyclization reactions and intermediates and other fragments useful in the synthesis of halichondrin macrolides
    发明人:FANG FRANCIS G; KIM DAE-SHIK; CHOI HYEONG-WOOK; CHASE CHARLES E
    权利人:EISAI R&D MAN CO LTD
    摘要:The invention provides methods for the synthesis of a halichondrin macrolides through a macrocyclization strategy. The macrocyclization strategy of the present invention involves subjecting a non-macrocyclic intermediate to a carbon-carbon bond-forming reaction (e.g., an olefination reaction (e.g., Horner-Wadsworth-Emmons olefination), catalytic Ring-Closing Olefin Metathesis, or Nozaki-Hiyama-Kishi reaction) to afford a macrocyclic macrolide. The invention also provides compounds useful as intermediates in the synthesis of a halichondrin macrolides and methods for preparing the same.

    专利号:US-11136335-B2
    优先权日:2016-06-30
    标题:Prins reaction and intermediates useful in the synthesis of halichondrin macrolides and analogs thereof
    发明人:CHASE CHARLES E; CHOI HYEONG-WOOK; ENDO ATSUSHI; FANG FRANCIS G; KIM DAE-SHIK
    权利人:EISAI R&D MAN CO LTD
    摘要:The invention provides methods for the synthesis of a halichondrin macrolides or analogs thereof through a cyclization reaction strategy. The strategy of the present invention involves subjecting an intermediate to Prins reaction conditions to afford a macrolide. The invention also provides compounds useful as intermediates in the synthesis of a halichondrin macrolides or analogs thereof and methods for preparing the same.

    专利号:US-2025188046-A1
    优先权日:2023-12-08
    标题:Ultrafast flow synthesis of functionalized sulfonyl fluorides and subsequent sufex connections via lithiated chemistry
    发明人:KIM DONG-PYO; KANG JI-HO
    权利人:POSTECH RES & BUSINESS DEV FOUND
    摘要:Disclosed are ultrafast flow synthesis of functionalized sulfonyl fluorides and subsequent SuFEx connections via lithiated chemistry. In detail, a method of synthesizing an ortho-functionalized benzenesulfonyl fluoride derivative, the method comprises (a) reacting a benzenesulfonyl fluoride derivative represented by structural formula 1 with an organolithium represented by structural formula 2, thus synthesizing an intermediate represented by structural formula 3 in reaction scheme 1 and (b) reacting the intermediate with an electrophile, thus synthesizing a compound represented by structural formula 4 or a compound represented by structural formula 4′. The present disclosure enables the synthesis of several functionalized sulfonyl fluorides within a few seconds under mild temperature conditions in addition to the chemistry of Sulfonyl Fluoride Exchange (SuFEx), which is a next-generation click chemistry, so that sulfonyl fluoride, the main reactant of the SuFEx reaction, can be efficiently secured.

    专利号:US-9783549-B2
    优先权日:2013-11-04
    标题:Macrocyclization reactions and intermediates useful in the synthesis of analogs of halichondrin B
    发明人:FANG FRANCIS G; KIM DAE-SHIK; CHOI HYEONG-WOOK; CHASE CHARLES E; LEE JAEMOON
    权利人:EISAI R&D MAN CO LTD
    摘要:The invention provides methods for the synthesis of eribulin or a pharmaceutically acceptable salt thereof (e.g., eribulin mesylate) through a macrocyclization strategy. The macrocyclization strategy of the present invention involves subjecting a non-macrocyclic intermediate to a carbon-carbon bond-forming reaction (e.g., an olefination reaction (e.g., Homer-Wadsworth-Emmons olefination), Dieckmann reaction, catalytic Ring-Closing Olefin Metathesis, or Nozaki-Hiyama-Kishi reaction) to afford a macrocyclic intermediate. The invention also provides compounds useful as intermediates in the synthesis of eribulin or a pharmaceutically acceptable salt thereof and methods for preparing the same.
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    合成参考文献


    摘要:Kostikov, R. R.; Khlebnikov, A. F.; Sokolov, V. V., Science of Synthesis, (2010) 47, 866.
    摘要:Lattanzi, A., Science of Synthesis: Stereoselective Synthesis, (2011) 3, 988.
    摘要:Lattanzi, A., Science of Synthesis: Stereoselective Synthesis, (2011) 3, 1000.
    摘要:Lattanzi, A., Science of Synthesis: Stereoselective Synthesis, (2011) 3, 991.
    摘要:Katsuki, T., Science of Synthesis: Water in Organic Synthesis, (2012) 1, 58.
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