Ok, now tell me this thing.
One pot chemistry with acyl chloride, is it possible? I've seen some procedures, where it is claimed that it's possible to inject the second reagent into the reaction when thionyl chloride is still there, in the reaction medium, in order to have the acyl chloride reacting with the next reagent in the same medium. I did not see any clear statements about it.
What considerations, in your opinion, should be done, in order to obtain a final product of acyl chloride condensation with something, in one reaction step?