I want to prepare monemer of Schiff bases of 2-amino thiazole , I prepared it according to puplished paper . but a dimer is formed . why????
N3- in 2-aminothiazole is stronger base, it attacks your aldehyde (adds to aldehyde) change to alcohol. The same carbon was then attacked by another thiazole molecule by replacing the OH gp.
thank you / Abdel-Nasser Ahmed El-Shorbagi
I want to prepare the monemer , I want the procedures for prepare the monemer
Schiff bases of 2-amino thiazole can be prepared by reacting it with an aldehyde using acetic acid catalyst.
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