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N,N-二苯基甲酰胺和N,N-二苯基乙酰胺的合成及光谱性质OA

Synthesis and Spectral Properties of N,N-Diphenylformamide and N,N-Diphenylethanamide

中文摘要英文摘要

以二苯胺为底物,N,N-二甲基甲酰胺和 N,N-二甲基乙酰胺为酰基化试剂,通过 Vilsmeier-Haack 反应,合成了 N,N-二苯基甲酰胺和 N,N-二苯基乙酰胺,并采用核磁共振氢谱(1 H NMR)、傅里叶变换红外光谱(FT-IR)及紫外可见吸收光谱(UV-Vis)表征其化学结构和光谱性质.实验结果表明,酰基化反应发生在亚氨基上.与二苯胺的 λmax 相比,N,N-二苯基甲酰胺和 N,N-二苯基乙酰胺的 λmax 显著蓝移.引入酰基破坏了二苯胺的共轭体系,导致相应产物的 λmax 显著蓝移.

Using diphenylamine as the starting material,and N,N-dimethylformamide and N,N-dimethylacetamide as the acylating reagents,N,N-diphenylformamide and N,N-diphenylacetamide were synthesized via the Vilsmeier-Haack reaction.The chemical structures and spectral prop-erties of N,N-diphenylformamide and N,N-diphenylacetamide were characterized by proton nuclear magnetic resonance spectroscopy(1 H NMR),Fourier transform infrared spectroscopy(FT-IR)and ultraviolet-visible absorption spectroscopy(UV-Vis).The results showed that the acylation reaction occurred at the imino group.Compared with the maximum absorption wavelength(λmax)of diphenylamine,the λmax values of N,N-diphenylformamide and N,N-diphenylacetamide exhibited a significant blue shift.The introduction of the acyl group disrupted the conjuga-tion of diphenylamine,leading to the obvious blue shift of the λmax of the corresponding products.

胡益波;刘意

贵州师范学院 化学与材料学院,贵州 贵阳 550018贵州师范学院 化学与材料学院,贵州 贵阳 550018

化学化工

二苯胺Vilsmeier-Haack反应结构表征光谱分析N,N-二苯基甲酰胺N,N-二苯基乙酰胺

DiphenylamineVilsmeier-Haack ReactionStructural CharacterizationSpectral AnalysisN,N-DiphenylformamideN,N-Diphenyle-thanamide

《云南化工》 2026 (8)

27-30,4

贵州师范学院2024年国家级大学生创新创业训练计划(2024142230453).

10.3969/j.issn.1004-275X.2026.08.07

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