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Preparation and properties of isomeric N-(4-substituted benzylidene)-4-ethynylanilines and 4-substituted N-(4-ethynylbenzylidene)anilines

机译:N-(4-取代的亚苄基)-4-乙炔基苯胺和4-取代的N-(4-乙炔基亚苄基)苯胺的异构体的制备和性质

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摘要

4-Substituted N-(4-ethynylbenzylidene)anilines (4-HC=C-C6H4-CH=N-C6H4-4-R; R = Me, t-Bu, OMe, F, Cl, Br, I, CF3 and NO2) have been prepared by condensation of 4-ethynylbenzaldehyde with appropriate anilines under mild conditions in good yields. The products obtained were fully characterized by GC-MS, IR, NMR and UV-VIS spectroscopies and their properties were compared with a series of 4-ethynyl-N-(4-substituted benzylidene)anilines (4-HC=C-C6H4-N=CH-C6H4-4-R; R = H, Me, t-Bu, F, Br, NO2, CN, NMe2). The influence of substituent R on spectroscopic characteristics is discussed. [References: 20]
机译:4-取代的N-(4-乙炔基亚苄基)苯胺(4-HC = C-C6H4-CH = N-C6H4-4-R; R = Me,t-Bu,OMe,F,Cl,Br,I,CF3和在温和的条件下,通过4-乙炔基苯甲醛与适当的苯胺缩合制备高收率的二氧化氮。通过GC-MS,IR,NMR和UV-VIS光谱对所得产物进行了充分表征,并将其性质与一系列4-乙炔基-N-(4-取代亚苄基)苯胺(4-HC = C-C6H4- N = CH-C6H4-4-R; R = H,Me,t-Bu,F,Br,NO 2,CN,NMe 2)。讨论了取代基R对光谱特性的影响。 [参考:20]

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