well my starting material contains t-BOC protected amine group that means i cannot use DMAP base for deprotonation as it's workup involves addition of HCl. SO could anyone please suggest me which reagent i can used for my reaction.
It is still possible to use DMAP, you can just remove the DMAP by another way like chromatography. Other possible alternatives include polymer supported DMAP, inorganic bases may also be possible depending on the reaction, or low boiling organic bases like triethylamine or pyridine although removing them on the rotavap may not be so straightforward.
Perhaps aqueous washes with a weaker acid (other than HCl) could be used to reove DMAP without deprotecting the Boc amine. Acetic or citric come to mind.
One thing...Whether your boc amine comound is sensitive to HCl? Or else you can use Dioxane.HCl/Diethyl Ether.HCl/methanol.HCl in dichloromethane at 0 oC.
In most of the above cases, HCl workup is required to remove organic bases(TEA, Pyridine etc.,) ....feeling doubt with DBU and DABCO or inorganic bases.
Catalytic DMAP is used in combination with a base to accelerate a reaction such a Boc-protection, acylation etc. If you want for deprotonation you have to use different bases depending on substrate. But DMAP could be easily removable through column chromatography.