Step 1: Recall what aspirin is.
Aspirin is the common name of acetylsalicylic acid. The word acetyl tells us an acetyl group \((CH_3CO-)\) has been put on.
Step 2: Understand acetylation.
Acetylation means replacing the hydrogen of a phenolic \(-OH\) group with an acetyl group, usually using acetic anhydride or acetyl chloride.
Step 3: Find the starting material.
To make acetylsalicylic acid we must start from salicylic acid. Salicylic acid is 2-hydroxybenzoic acid, which has both a phenolic \(-OH\) and a \(-COOH\) group.
Step 4: Acetylate the right group.
The phenolic \(-OH\) of 2-hydroxybenzoic acid is acetylated, turning \(-OH\) into \(-OCOCH_3\), giving aspirin.
Step 5: Conclude.
So aspirin is obtained by the acetylation of 2-hydroxybenzoic acid (salicylic acid).
\[ \boxed{\text{2-Hydroxybenzoic acid}} \]