Electric Literature of 6574-15-8, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.6574-15-8, Name is 1-(4-Nitrophenyl)piperidine, molecular formula is C11H14N2O2. In a article£¬once mentioned of 6574-15-8
Aromatic Nucleophilic Substitution of Halobenzenes with Amines under High Pressure
The nucleophilic substitution reactions of aromatic halides having electron-attracting groups on ortho or para position with various primary and secondary amines were accelerated by high pressure to give the corresponding N-substituted anilines in high yields.The bulkiness of amines affects its reactivity to lower the yields of the products.Although the secondary amines are usually less reactive than primary amines, cyclic secondary amines such as morpholine, piperidine, and pyrrolidine were found very reactive. 1,4-Diazabicyclo<2.2.2>octane and quinuclidine gave N-quarternary ammonium halides in high yields in contrast to the low reactivity of acyclic tertiary amines.Dichloro- and trichloro-nitrobenzenes also react with diethylamine, pyrrolidine, and morpholine to give mono-, di-, and trisubstitution products depending upon the amount of amine and the position of nitro group in these chlorides.
We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 6574-15-8, and how the biochemistry of the body works.Electric Literature of 6574-15-8
Reference£º
Piperidine – Wikipedia,
Piperidine | C5H15289N – PubChem