The Reimer-Tiemann reaction is a chemical reaction that involves the formylation of phenols. It is used to introduce an aldehyde group (-CHO) at the ortho or para position to the hydroxyl group (-OH) on an aromatic ring. The reaction uses chloroform (CHCl₃) and a strong base like sodium hydroxide (NaOH) to produce salicylaldehyde.
The general reaction is as follows:
\[ \text{Phenol} + \text{CHCl}_3 + \text{NaOH} \rightarrow \text{Salicylaldehyde} \]
This reaction proceeds by the formation of a dichlorocarbene intermediate, which then reacts with the phenol to give the ortho and para products, typically with the para product being the major one.
