1. Grignard reagent of o,a-dichlorotoluene is reacted with acetone.
2. Tetrtiary alcohol of last step is reacted with NaCN in glacial HOAc.
3. Product of the last step (presumably nitrile) is boiled in mineral acid.
I know Hofmann rearrangement can convert an amide to an amine in base and Br2.
How exactly is the above reaction get a cyanide functional group into an amine just by boiling it in acid?
Obviously pedantic point i mean alkaloid amine not ammonia by amide hydrolysis.
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