📜(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
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
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.