CAS: 21906-39-8; 1-[3-(Trifluoromethyl)Phenyl]-2-Propanone

该化合物是一种氟芳香酮化合物,其特点是在苯环的元位置上有一个三氟甲基(-CF3)组,这种结构特征增强了其电子提取特性,使其在合成有机化学中作为制药,农用化学品和特殊材料的中间体具有宝贵价值.氯酮功能(丙基-2-1)提供了一个反应场,供进一步衍生,如凝聚或减少反应.三氟甲基组改善了代谢稳定性和脂质,这对药物设计有利.其高纯度和定义明确的结构确保了研究和工业应用的再生性.该化合物通常在受控制的条件下处理,因为其具有再活性.

结构式图片

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ECHA物质C&L通报REACH预注册

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CAS号108-22-5 醋酸异丙烯酯 | CAS号98-16-8 间三氟甲苯胺 | CAS号401-78-5 间溴三氟甲苯 | CAS号78-95-5 氯丙酮 | CAS号368-79-6 3-Isopropenylbe... | CAS号108-24-7 乙酸酐 | CAS号705-29-3 3-三氟甲基氯苄 | CAS号713-71-3 2-[3-(trifluoro... | CAS号1139705-23-9 3-(trifluoromet... | CAS号67-64-1 丙酮 | CAS号458-24-2 左芬氟拉明 | CAS号19036-73-8 (S)-1-(3-三氟甲基苯基... | CAS号31173-14-5 2-[[1-methyl-2-... | CAS号38060-02-5 1-[m-(Trifluoro... | CAS号52271-40-6 N-ethyl-N-[1-[3...

合成工艺路线路线简述

    📜(E)-1-Phenyl-N-{1-[3-(Trifluoromethyl)Phenyl]Prop-1-En-2-Yl}Methanimine置于水,草酸体系中,化学反应生成3-三氟甲基苯丙酮
    参考文献:α-Aminophosphonates: I. Synthesis Of 2-Azadienes And Their Hydrolysis To Carbonyl Compounds
    标题:α-Aminophosphonates: I. Synthesis Of 2-Azadienes And Their Hydrolysis To Carbonyl Compounds
    摘要:
    Doi:10.1055/s-1977-24449

    海关参考信息

    专利信息


    专利号:US-5811586-A
    优先权日:1996-05-29
    标 题 :Process for manufacturing 1-(3-trifluoromethyl)-phenyl-propan-2-one intermediate in the synthesis of the fenfluramine
    发明人:CANNATA VINCENZO; GALBIATI BARBARA; SPREAFICO ANGELO
    权利人:ALFA CHEM ITAL
    摘要:A process for manufacturing 1-(3-trifluoromethyl)phenyl-propan-2-one intermediate in the synthesis of the anorexic drug fenfluramine consists of reacting the diazonium salt of 3-trifluoromethylaniline with isopropenyl acetate in a polar solvent in the presence of a catalytic amount of a cuprous salt and, optionally, of a base and purifying the crude product through the bisulfite complex or distillation under vacuum.

    专利号:EP-1075534-B8
    优先权日:1998-03-11
    标 题 :Improvements in the enzymatic synthesis of chiral amines
    发明人:WU WEI; BHATIA MOHIT B; LEWIS CRAIG M; LANG WEI; WANG ALICE; MATCHAM GEORGE W
    权利人:CELGRO
    摘要:2-Aminopropane is used as the amine donor in the stereoselective synthesis of a chiral amine from a ketone with a transaminase. In a typical embodiment, (S)-1-methoxy-2-aminopropane is prepared by bringing methoxyacetone into contact with a transaminase in the presence of 2-aminopropane as an amine donor until a substantial amount of methoxyacetone is converted to (S)-1-methoxy-2-aminopropane and 2-aminopropane is converted to acetone. In a second embodiment, L-alanine is prepared by bringing pyruvic acid into contact with a transaminase in the presence of 2-aminopropane as an amine donor.

    专利号:US-5808156-A
    优先权日:1997-04-28
    标题 :Process for the production of the isomers (R) and (S)-α-methyl-3(trifluoromethyl)benzeneethanamine
    发明人:CANNATA VINCENZO; GALBIATI BARBARA; FERRARIO TIZIANO
    权利人:ALFA CHEM ITAL
    摘要:Process for the production of the isomers (R) and (S)-α-methyl-3-(trifluoromethyl)benzeneethanamine, the second being useful as intermediate in the synthesis of the anorexic drug dexfenfluramine (INN), which comprises carrying out a stereospecific reductive amination of 1-(3-trifluoromethyl)phenyl-2-propanone with (R) or (S)-α-methylbenzylamine under a hydrogen atmosphere in the presence of a catalyst and debenzylating the resulting diastereoisomer (R),(R) or (S),(S)-N-(1-phenylethyl)-α-methyl-3-(trifluoromethyl)benzeneethanamine by treatment with hydrogen and a catalyst.

    专利号:US-2018208543-A1
    优先权日:2017-01-26
    标 题 :New method for synthesis of fenfluramine, and new compositions comprising it
    发明人:PALOMBI GIOVANNI; ZAGAMI MICHAEL
    权利人:FRAU PHARMA S R L
    摘要:A new process for preparing the fenfluramine molecule and new compositions containing fenfluramine obtainable with the claimed process.

    专利号:EP-3170807-A1
    优先权日:2015-11-23
    标题:New method for synthesis of fenfluramine, of isomers therof and/or of analogs thereof, and new compositions comprising it

    专利号:EP-0810195-A1
    优先权日:1996-05-29
    标题:Process for manufacturing 1-(3-trifluoromethyl)phenyl-propan-2-one intermediate in the synthesis of the fenfluramine

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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:Development Of General Methods For The Synthesis Of New Substituted Allyl Bromides As Promising Alkenylating Agents
    作者:A. I. Moskalenko,V. I. Boev |发布日期:2014.7
    摘要:A General Procedure Has Been Developed For The Synthesis Of Hitherto Unknown Substituted Allyl Bromides. The Procedure Includes Preparation Of The Corresponding α,β-Unsaturated Carboxylic Acid Esters From Accessible Ketones According To The Horner-Emmons Reaction, Reduction Of These Esters With Diisobutylaluminum Hydride To Allylic Alcohols, And Substitution Of The Hydroxy Group By Bromine By The Action

    合成参考文献


    摘要:Wu, X.; Xiao, J., Science of Synthesis: Water in Organic Synthesis, (2012) 1, 272.
    摘要:Steiner, K.; Glieder, A.; Gruber-Khadjawi, M., Science of Synthesis: Biocatalysis in Organic Synthesis, (2015) 2, 11.
    摘要:Steiner, K.; Glieder, A.; Gruber-Khadjawi, M., Science of Synthesis: Biocatalysis in Organic Synthesis, (2015) 2, 6.
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