is the active ingredient in many sulfonation reactions. Typical conditions involve heating the aromatic compound with sulfuric acid: :
Sulfur trioxide or its protonated derivative is the actual
electrophile in this electrophilic aromatic substitution. To drive the equilibrium, dehydrating agents such as
thionyl chloride can be added:
Chlorosulfuric acid is also an effective agent: : In contrast to
aromatic nitration and most other electrophilic aromatic substitutions this reaction is
reversible. Sulfonation takes place in concentrated acidic conditions and desulfonation is the mode of action in a dilute hot aqueous acid. The reaction is very useful in
protecting the aromatic system because of this reversibility. Due to their
electron withdrawing effects, sulfonate protecting groups can be used to prevent electrophilic aromatic substitution. They can also be installed as
directing groups to affect the position where a substitution may take place. ==Specialized sulfonation methods==