N-bromobutanimide → 1-Butanone, 1-[4-(1-bromo-1-methylethyl)phenyl]-4-chloro-

HRID 1066463Notes

Reaction equation

HRID 1066463 reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][C:5]([C:7]1[CH:12]=[CH:11][C:10]([CH:13]([CH3:15])[CH3:14])=[CH:9][CH:8]=1)=[O:6].[Br:16]N1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl.CC(N=NC(C#N)(C)C)(C#N)C>[Br:16][C:13]([C:10]1[CH:9]=[CH:8][C:7]([C:5](=[O:6])[CH2:4][CH2:3][CH2:2][Cl:1])=[CH:12][CH:11]=1)([CH3:15])[CH3:14]

Participants

5

Conditions

Temperature
85 °C

Procedure

Dissolve 4-chloro-1-(4-isopropyl-phenyl)-butan-1-one (5.00 g, 22.2 mmol) and N-bromosuccinimide (4.1 g, 23.0 mmol) in carbon tetrachloride (25 mL) and add AIBN radical initiator (300 mg). Stir and maintain under a nitrogen atmosphere at 80-90° C. or optionally irradiate with a sunlamp until a vigorous exotherm occurs at which point momentarily remove until reflux subsides and then reapply the heat. Reflux for 30 minutes and add another potion of N-bromosuccinimide (100 mg) while maintaining reflux and reflux an additional 15 minutes. Cool to room temperature and precipitate the succinimide from the solution by allowing to stand overnight. Filter and wash the succinimide (2.25 g) with carbon tetrachloride (20 mL). Combine the filtrates and evaporate the solvent in vacuo to give the title compound as a yellow oil (6.80 g, 100%).

Workup

  1. customoptionally irradiate with a sunlamp until a vigorous exotherm
  2. custommomentarily remove
  3. temperatureuntil reflux subsides
  4. temperatureReflux for 30 minutes
  5. additionadd another potion of N-bromosuccinimide (100 mg)
  6. temperaturewhile maintaining
  7. temperaturereflux
  8. temperaturereflux an additional 15 minutes
  9. temperatureCool to room temperature
  10. customprecipitate the succinimide from the solution
  11. filtrationFilter
  12. washwash the succinimide (2.25 g) with carbon tetrachloride (20 mL)
  13. customCombine the filtrates and evaporate the solvent in vacuo

Sources & evidence

ORD record
ord-4da7117e90e24063a8df3c1b06a26c13
Source dataset
uspto-grants-2001_06
Patent number
US06242606B1

Reaction notes

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