CAS: 13170-43-9; (Trimethylsilyl)Methylmagnesium Chloride

该化合物是一种反应性很强的灰色试剂,通常在四氢呋喃(THF)中作为1.3M溶液供应.这种试剂广泛用于有机合成,以引入(三甲基硅)甲基组,从而能够在各种变异中形成碳-碳结层.J & KSearal确保高纯度和稳定性,使其适合敏感反应.它与高温聚氟酯作为溶剂的兼容性会提高溶性与再活性,促进碳基化合物和其他电极的高效核分裂性添加.标准化浓度允许精确的异异异谱控制,改进合成应用中的再复制性.建议在惰性条件下进行适当处理,以保持试剂的完整性.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

Chloromethyltrimethylsilane diethyl ether magnesium3-trimethylsilyl-1-propanol bis(trimethylsilyl)methane chloromethyl(dimethyl)(trimethylsilylmethyl)silane 2-trimethylsilylacetonitrile

合成工艺路线路线简述

  • 合成目标产物 Trimethylsilylmethylmagnesium Chloride 主要起始原料 Magnesium And Chloromethyltrimethylsilane
  • (文献来源)合成步骤主要原料 Magnesium 和 Chloromethyltrimethylsilane
氯甲基三甲基硅烷置于magnesium体系中,用 四氢呋喃 用作溶剂,化学反应 12.0H,反应生成(三甲基硅基)甲基氯化镁
参考文献:Ib-00208糖苷配基的全合成
标题:Ib-00208糖苷配基的全合成
摘要:Ib-00208糖苷配基的总合成使用新开发的方法从苯并环丁烯酮向多环1,4-二加氧的氧杂蒽开发,共分22个步骤完成.最初在几种模型系统上建立了氧杂蒽酮的通用性,然后才成功地将其用于天然产物的六环核的构建.还开发了一种使用闭环复分解(rcm)的有角度稠合苯并环丁烯酮的新方法,并且可能具有通用性.
Doi:10.1016/j.Tet.2015.05.024

专利信息


专利号:US-2013196019-A1
优先权日:2010-03-18
标 题:Silicon-containing block co-polymers, methods for synthesis and use
发明人:WILLSON C GRANT; BATES CHRISTOPHER M; STRAHAN JEFFREY; ELLISON CHRISTOPHER JOHN; MUELLER BRENNEN
权利人:WILLSON C GRANT; BATES CHRISTOPHER M; STRAHAN JEFFREY; ELLISON CHRISTOPHER JOHN; MUELLER BRENNEN; NAT UNIVERSITY OF SINAPORE
摘要:The present invention describes the synthesis of silicon-containing monomers and copolymers. The synthesis of a monomer, trimethyl-(2-methylenebut-3-enyl)silane (TMSI) and subsequent synthesis of diblock copolymer with styrene, forming polystyrene-block-polytrimethylsilyl isoprene, and synthesis of diblock copolymer Polystyrene-block-polymethacryloxymethyltrimethylsilane or PS-b-P(MTMSMA). These silicon containing diblock copolymers have a variety of uses. One preferred application is as novel imprint template material with sub-100 nm features for lithography.

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-12139504-B2
优先权日:2022-08-09
标 题:Vanadium alkylidene complex, synthesis and use thereof
发明人:BUKHRYAKOV KONSTANTIN; BELOV DMITRY
权利人:BUKHRYAKOV KONSTANTIN; BELOV DMITRY; THE FLORIDA INTERNATIONAL UNIV BOARD OF TRUSTEES
摘要:The subject invention provides catalytical compounds/complexes, compositions comprising such compound/complex, synthesis of the compounds/complexes, and methods of using such compounds/complexes as catalysts in, for example, RCM reactions. Specifically, the subject invention provides the synthesis of the first catalytically active V oxo alkylidene, VO(CHSiMe 3 )(PEt 3 ) 2 Cl, which exhibits superior performance compared to other analogs.

专利号:US-7026339-B2
优先权日:2003-11-07
标题 :Inhibitors of HCV NS5B polymerase
发明人:YANG FAN; ZHANG BO; WICNIENSKI NANCY ANNE; PFEFFERKORN JEFFREY ALLEN; GREENE MEREDITH L; CHEN KE; NUGENT RICHARD A; REDING MATTHEW TODD; KELLY ROBERT CHARLES; MITCHELL MARK A; FUNK LEE A; HEIER III RICHARD FREDERICK; ANDERSON REBECCA MERRY
权利人:YANG FAN; ZHANG BO; WICNIENSKI NANCY ANNE; PFEFFERKORN JEFFREY ALLEN; GREENE MEREDITH L; CHEN KE; NUGENT RICHARD A; REDING MATTHEW TODD; KELLY ROBERT CHARLES; MITCHELL MARK A; FUNK LEE A; HEIER III RICHARD FREDERICK; ANDERSON REBECCA MERRY
摘要:The present invention relates to compounds, process for their synthesis, compositions and methods for the treatment and prevention of hepatitis C virus (HCV) infection. In particular, the present invention provides novel compounds, pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment or prevention of HCV infection. The present invention also provides processes and intermediates for the synthesis of these compounds.

专利号:US-11897827-B1
优先权日:2022-11-22
标 题 :Carbon isotope exchange mediated by vanadium complexes
发明人:BUKHRYAKOV KONSTANTIN
权利人:BUKHRYAKOV KONSTANTIN; THE FLORIDA INTERNATIONAL UNIV BOARD OF TRUSTEES
摘要:The subject invention provides catalytical compounds/complexes, compositions comprising such compound/complex, synthesis of the compounds/complexes, and methods of using such compounds/complexes as catalysts in, for example, carbon isotope exchange (CIE) on target bioactive molecules. Methods that allow CIE directly on drug candidates are of great importance to chemistry, biology, and medicine. Especially valuable are catalytic procedures that rely on a limited collection of available labeled materials. The instant method comprises converting a methyl group to terminal â•?CH2 utilizing transfer dehydrogenation catalysts to enable V-based olefin metathesis, followed by a hydrogenation step. The one-pot strategy allows the formal methylation/demethylation sequence and can be applied to an assortment of alkyl-containing compounds.

专利号:US-9663594-B2
优先权日:2014-05-15
标 题 :Synthesis of aryl coupled bis phenoxides and their use in olefin polymerization catalyst systems with activator-supports
发明人:HLAVINKA MARK L
权利人:CHEVRON PHILLIPS CHEMICAL CO LP; CHEVRON PHILIPS CHEMICAL COMPANY LP
摘要:Disclosed herein are methods of making bis(phenol) ligand compounds and transition metal bis(phenolate) compounds. The transition metal bis(phenolate) compounds can be used as components in catalyst systems for the polymerization of olefins.
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✅ COA系统入驻 | 共享模式

主要参考文献

参考标题:A Novel And Versatile Silicon-Derived Linkage Agent, 4-[1-Hydroxy-2-(Trimethylsilyl)Ethyl]Benzoic Acid, Compatible With The Fmoc/t-Bu Strategy For Solid Phase Synthesis Of C-Terminal Peptide Acids
作者:Hann-Guang Chao,Michael S. Bernatowicz,Paul D. Reiss,Clifford E. Klimas,Gary R. Matsueda |发布日期:1994.3
摘要:Solid-Phase Peptide Synthesis. With The Development Of A Versatile Silicon-Based Linkage Agent, «sac», 4-[1-Hydroxy-2-(Trimethylsilyl)Ethyl] Benzoic Acid (1), For The Production Of Peptide C-Terminal Acids, These Problems Have Been Successfully Solved. Demonstration Of The Advantages Of Using Sac Linker Was Provided By Synthesizing A C-Terminal Tryptophan-Containing Dodecapeptide And A C-Terminal Proline-Containing

合成参考文献


摘要:Reissig, H.-U.; Zimmer, R., Science of Synthesis, (2008) 44, 328.
摘要:Wong, Y.-S., Science of Synthesis, (2009) 46, 627.
摘要:Amatore, M.; Aubert, C.; Malacria, M.; Petit, M., Science of Synthesis Knowledge Updates, (2012) 3, 53.
摘要:Amatore, M.; Aubert, C.; Malacria, M.; Petit, M., Science of Synthesis Knowledge Updates, (2012) 3, 96.
摘要:Ager, D. J., Science of Synthesis, (2010) 47, 89.
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