C1(=[N:7]O)CCCCC1.[S:9](=[O:13])(=[O:12])([OH:11])[OH:10].OS(O)(=O)=O.O=S(=O)=O.S(O)(O)(=O)=O.[C:28]1(=[O:35])[NH:34][CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]1.[NH3:36]>>[C:28]1(=[O:35])[NH:34][CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]1.[S:9]([O-:13])([O-:12])(=[O:11])=[O:10].[NH4+:7].[NH4+:36]The Beckmann rearrangement of the cyclohexanone oxime is carried out with sulfuric acid or oleum. The caprolactam sulfate prepared in this case and excess sulfuric acid are reacted with ammonia to give caprolactam and ammonium sulfate.
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