Hydrogen Bromide → (3RS)-3-amino-4,4-dimethyl-pentan-2-one hydrobromide
Reaction equation
C(OC([NH:6][CH:7]([C:11]([CH3:14])([CH3:13])[CH3:12])[C:8](=[O:10])[CH3:9])=O)C.[BrH:15]>>[BrH:15].[NH2:6][CH:7]([C:11]([CH3:14])([CH3:13])[CH3:12])[C:8](=[O:10])[CH3:9]Participants
3
Procedure
N-ethoxycarbonyl-3-amino-4,4-dimethyl-pentan-2-one (203 mg) is dissolved in 48% aqueous hydrobromic acid (4 ml) and the solution is stirred under reflux for 6 hours. The reaction mixture is then evaporated under reduced pressure to give a solid residue, that is further purified by recrystallisation (from ethanol/diethylether) to afford 149 mg of pure (3RS)-3-amino-4,4-dimethyl-pentan-2-one hydrobromide (m.p. 218°-220° C.)
Workup
- temperatureunder reflux for 6 hours
- customThe reaction mixture is then evaporated under reduced pressure
- customto give a solid residue, that
- customis further purified by recrystallisation (from ethanol/diethylether)
Sources & evidence
- ORD record
- ord-46d3bf04f9f64d0fb7cfa517cb176bc7
- Source dataset
- uspto-grants-1995_05
- Patent number
- US05418238
Reaction notes
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