Limitations of Friedel craft acylation
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Not given by nh2 oh no2 and highly deactivated ring
3* form alkene and
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Acylation can only be used to give ketones. This is because HCOCl decomposes to CO and HCl under the reaction conditions.
Deactivated benzenes are not reactive to Friedel-Crafts conditions, the benzene needs to be as or more reactive than a mono-halobenzene (see substituent effects)
The Lewis acid catalyst AlCl3 often complexes to aryl amines making them very unreactive.
Amines and alcohols can give competing N or O acylations rather than the require ring acylation.
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