CAS: 651-80-9; 1,2,4,5-Tetrafluoro-3-(Trifluoromethyl)Benzene

该化合物是一种氟芳烃化合物,其特点是其高热和化学稳定性.多种氟替代成分的存在增强了其抗氧化和降解的抗药性,使其适合农业化学和制药合成方面的要求应用.其电排剂特性有利于核生殖替代反应,而其亲脂性则提高了有机基质的溶性.该化合物极分性和惰性也使它作为包括液体晶体和特殊聚合物在内的先进材料的建筑块具有价值. 处理要求对氟有机物采取标准防范措施,但其定义明确的再活性特征则确保合成工作流程的一贯性能.

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CAS号617-86-7 三乙基硅烷 | CAS号434-64-0 八氟甲苯 | CAS号17823-46-0 4-三氟甲基-2,3,5,6-四氟溴苯 | CAS号122571-42-0 4-trimethylsily... | CAS号40885-89-0 4-氯-2,3,5,6-四氟三氟甲基苯 | CAS号1868-85-5 (α,α,α,2,3,5,6-... | CAS号107-05-1 氯丙烯 | CAS号7732-18-5 水 | CAS号54899-60-4 ((4-trifluorome... | CAS号654-87-5 2,3,5-三氟苯甲酸 | CAS号652-18-6 2,3,5,6-四氟苯甲酸 | CAS号17823-46-0 4-三氟甲基-2,3,5,6-四氟溴苯 | CAS号79150-81-5 5-bromo-1,3,3,4... | CAS号40885-89-0 4-氯-2,3,5,6-四氟三氟甲基苯 | CAS号87905-89-3 5-chloro-1,3,3,... | CAS号53700-73-5 1,2,4,5-tetrafl... | CAS号61794-43-2 1,2,4,5-tetrafl... | CAS号61794-47-6 3-[2,3,5,6-tetr...

合成工艺路线路线简述

  • 合成目标产物 2,3,5,6-Tetrafluorobenzotrifluoride 主要起始原料 4-Trifluoromethyl-2,3,5,6-Tetrafluorothiophenol
  • (文献来源)合成步骤主要原料 4-Trifluoromethyl-2,3,5,6-Tetrafluorothiophenol
八氟甲苯置于(Hc[(Cme)N(2,4,6-Me3C6H2)]2)Alh2体系中,用 氘代苯 作为反应溶剂,化学反应 336.0H,反应生成 2,3,5,6-四氟三氟甲苯
参考文献:Piii/pv 合成循环中的往返氧化加成,配体复分解和还原消除
标题:Piii/pv 合成循环中的往返氧化加成,配体复分解和还原消除
摘要:报道了芳基 Cf 取代的合成循环,包括在 Cs 对称磷三酰胺 (1,P{n[o-Nme-C6H4]2}) 上的氧化加成,配体复分解和还原消除.1 与全氟芳烃 (Arf-F) 的反应导致 Cf 氧化加成,反应生成氟正膦 1•[f][arf].通过用 Dibal-H 处理,P-氟取代基被交换为氢化物,反应生成氢化正膦 1•[h][arf].1•[h][arf] 的加热通过 Arf-H 的 Ch 还原消除再生 1,其中实验和计算研究建立了协调但高度异步的机制.结果提供了在单个主要基团位点处的基本机械芳基 Cx 取代步骤的完整三元组的充分表征的例子.
DOI:10.1021/jacs.0C07580

海关参考信息

专利信息


专利号:US-2012215002-A1
优先权日:2009-10-09
标 题:Synthesis of optically active intermediate for the preparation of montelukast
发明人:LEFORT LAURENT
权利人:LEFORT LAURENT
摘要:The present invention relates to the synthesis of optically active alcohols by means of enantioselective hydrogenation of ketones in biphasic systems. In particular the present invention relates to the synthesis of an optically active alcohol of general formula (1).

专利号:US-11999757-B2
优先权日:2017-11-01
标 题:Synthesis of boronate ester derivatives and uses thereof
发明人:BOYER SERGE HENRI; HECKER SCOTT J; VERZIJL GERARDUS K M; HERMSEN PETRUS J
权利人:MELINTA SUBSIDIARY CORP
摘要:Disclosed herein are methods for the preparation of boronate derivatives in the synthesis of antimicrobial compounds and uses thereof. Disclosed herein includes method of making a compound of Formula (B) by reducing the ketone group of the keto-ester compound of Formula (A), and the reduction can be performed using a Ruthenium based catalyst system or using an alcohol dehydrogenase bioreduction system.

专利号:US-2007260076-A1
优先权日:2003-12-05
标 题:Practical, Cost-Effective Synthesis of Ubiquinones
发明人:LIPSHUTZ BRUCE H; BERL VOLKER; SHEIN KARIN; WETTERICH FRANK
权利人:LIPSHUTZ BRUCE H; BERL VOLKER; SHEIN KARIN; WETTERICH FRANK
摘要:The present invention provides a convergent method for the synthesis of ubiquinones and ubiquinone analogues. Also provided are precursors of ubiquinones and their analogues that are useful in the methods of the invention. The invention further provides an improved method for the carboalumination of alkyne substrates.

专利号:US-2006167289-A1
优先权日:2003-12-05
标题 :Practical, cost-effective synthesis of ubiquinones
发明人:LIPSHUTZ BRUCE H; BERL VOLKER; SCHEIN KARIN; WETTERICH FRANK
权利人:ZYMES LLC
摘要:The present invention provides a convergent method for the synthesis of ubiquinones and ubiquinone analogues. Also provided are precursors of ubiquinones and their analogues that are useful in the methods of the invention. The invention further provides an improved method for the carboalumination of alkyne substrates.

专利号:US-10669292-B2
优先权日:2014-05-05
标 题 :Synthesis of boronate salts and uses thereof
发明人:HECKER SCOTT; BOYER SERGE
权利人:REMPEX PHARMACEUTICALS INC
摘要:Disclosed herein are boronate intermediates in the synthesis of antimicrobial compounds and the use and preparation thereof. Some embodiments relate to crystalline boronate salt derivatives and their use in the synthesis of therapeutic compounds.

专利号:US-6852895-B2
优先权日:2000-08-15
标题:Practical, cost-effective synthesis of CoQ10
发明人:LIPSHUTZ BRUCE H; MOLLARD PAUL
权利人:ZYMES INC
摘要:The present invention provides a convergent method for the synthesis of ubiquinones and ubiquinone analogues. Also provided are precursors of ubiquinones and their analogues that are useful in the methods of the invention.
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主要参考文献

参考标题:Synthesis Of PyridineN-Oxide-Bf2Cf3Complexes And Their Fluorescence Properties
作者:Tomoaki Nishida,Aiko Fukazawa,Eriko Yamaguchi,Hiroya Oshima,Shigehiro Yamaguchi,Motomu Kanai,Yoichiro Kuninobu |发布日期:2014.4
摘要:Pyridine N‐oxide-Bf2Cf3 And -Bf2C2F5 Complexes And Their Derivatives Were Synthesized. Most Of The Complexes Show Fluorescence Both In Solution And In The Solid State. By Expanding The π‐conjugated Skeleton, The Color Of The Fluorescence Could Be Changed Dramatically. A Fluorophore With A High Solvent Dependency Could Also Be Produced. Since Such Compounds Can Be Synthesized On A Gram Scale In High

合成参考文献


摘要:Kwiecień, H., Science of Synthesis Knowledge Updates, (2014) 4, 133.
摘要:Harris, P. A., Science of Synthesis Knowledge Updates, (2021) 3, 55.
摘要:Zhang, M.; Su, W., Science of Synthesis: Catalytic Transformations via CH Activation, (2015) 1, 113.
摘要:Bellina, F.; Perego, L. A., Science of Synthesis: Catalytic Oxidation in Organic Synthesis, (2017) 1, 754.
摘要:Ghosh, B.; Maleczka, R. E., Jr., Science of Synthesis: Catalytic Reduction in Organic Synthesis, (2017) 1, 362.
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