I don't know if your stoichiometry is right, however there are at least two things you must consider if you attempt that:
1. this reaction will evolve a LOT of heat
2. have you checked how soluble HCl is in EtOAc? Because you might even manage to generate tons of HCl, but if your solvent can't take it, the acid will just fly away (and dissolve your face, presumably).
As far as I'm aware, when you use AcCl to make HCl, you generally use a strong eccess of alcohol so that the alcohol can dissolve the HCl.
In some special cases you can even add the AcCl to a mixture of alcohol and the product you want to react with HCl. There are industrial processes using that.