This answer is not correct. You have either confused this compound with the malonic ester synthesis or reacted the base with the methyl group, which has much less acidic hydrogen atoms.

If you thought that this was a malonic ester synthesis, you are probably trying to just memorize reactions without working them out and this leads to this type of mistake. Always try to work through all of the steps.

If you did an acid-base reaction at the methyl group, remember that the anion formed at the methylene position will have 2 favorable inductive interactions and resonance with both the ester carbonyl and the ketone and thus be much more stabile. If you did do the substitution at the methyl position, then you made a mistake in the mechanism for the ester hydrolysis/decarboxylation reaction because you should have ended up with the correct answer anyway...bummer, I cannot believe I didn't catch that before I made all the graphics.