I synthesized a series of tri-substituted imidazole derivatives. But the problem is percentage yield along with the impurities. So, how I can purify the compounds with a good yield without these two techniques. I tried the TLC with the solvent system (Benzene:Acetone, 8:2, v/v) and for column chromatography, I prewashed the column with DCM and methanol and then I used 5% w/w methanolic ammonia solution.

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