Hydrochloric Acid → Phenacylamine
Reaction equation
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:4].C1N2CN3CN(C2)C[N:12]1C3.Cl>C(Cl)(Cl)Cl>[NH2:12][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:4]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
2-Bromoacetophenone (18 g, 90 mmol) was dissolved in 900 m of chloroform. Hexamethylenetetraamine (13.87 g, 99 mmol) was added thereto and the reaction mixture was stirred at 60° C. for 4 hours. After stirring, the reaction mixture was cooled down to room temperature, filtered, and the collected precipitate was suspended in 180 m of ethanol. To the suspension thus obtained was added dropwise 90 m of conc. HCl, and the reaction mixture was stirred at room temperature for 18 hours. Then, the reaction mixture was filtered to remove a white precipitate, the filtrate was concentrated under reduced pressure to obtain a yellow solid. This solid was recrystallized from a mixture of methanol and ethyl acetate (1:50, v/v) to obtain 13 g of 2-aminoacetophenone as a yellow solid.
Workup
- stirringAfter stirring
- temperaturethe reaction mixture was cooled down to room temperature
- filtrationfiltered
- customTo the suspension thus obtained
- stirringthe reaction mixture was stirred at room temperature for 18 hours
- filtrationThen, the reaction mixture was filtered
- customto remove a white precipitate
- concentrationthe filtrate was concentrated under reduced pressure
- customto obtain a yellow solid
- customThis solid was recrystallized from a mixture of methanol and ethyl acetate (1:50
Sources & evidence
- ORD record
- ord-ea0b28de50524efbb0121fe8de00838f
- Source dataset
- uspto-grants-1999_07
- Patent number
- US05929103
Reaction notes
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