Propanal Hydroamination with p-Aminobenzoic Acid

被引:2
作者
Magdalinova, N. A. [1 ]
Volkova, T. G. [1 ]
Klyuev, M. V. [1 ]
Gruzdev, M. S. [2 ]
机构
[1] Ivanovo State Univ, Ivanovo, Russia
[2] Russian Acad Sci, Inst Solut Chem, Ivanovo 153045, Russia
关键词
Benzoic Acid; Enamine; Tautomeric Equilibrium; Separate Precipitate; Apparent Reaction Rate;
D O I
10.1134/S1070428010050052
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The propanal hydroamination was studied. It was found that the reaction in ethanol proceeded faster than in 2-propanol. By (1)H and (13)C NMR method the existence was proved of a tautomeric equilibrium in ethanol solution between 4-(propylideneamino)benzoic acid and its enamine form, 4-(prop-1-en-1-ylamino)benzoic acid.
引用
收藏
页码:634 / 636
页数:3
相关论文
共 10 条
[1]  
Barton D., 1979, Comprehensive Organic Chemistry, V3
[2]  
GORNOSTAEV LM, 1996, SOROSOVSKII OBRAZOVA, V4, P33
[3]  
Klyuev M.V., 2004, Catalytic Synthesis of Amines
[4]  
Klyuev M. V., 1991, THESIS MOSCOW
[5]  
KLYUEV MV, 2006, ROS KHIM ZH, V50, P93
[6]  
LUHRING P, 1989, J CHEM ENG DATA, V34, P250
[7]  
Mashkovskii M.D., 1993, LEKARSTVENNYE SREDST
[8]  
REICHARDT C, 1973, RASTVORITELI ORGANIC
[9]  
RICHTER F, 1951, BEILST, V14, P260
[10]  
RID R, 1966, PROPERTIES GASES LIQ