Hydrochloric Acid → Phenacylamine

HRID 583193Notes

Reaction equation

HRID 583193 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

5

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

  1. stirringAfter stirring
  2. temperaturethe reaction mixture was cooled down to room temperature
  3. filtrationfiltered
  4. customTo the suspension thus obtained
  5. stirringthe reaction mixture was stirred at room temperature for 18 hours
  6. filtrationThen, the reaction mixture was filtered
  7. customto remove a white precipitate
  8. concentrationthe filtrate was concentrated under reduced pressure
  9. customto obtain a yellow solid
  10. 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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