1-Bromo-3-fluorobenzene → HCID 14032496, compound

HRID 845638Notes

Reaction equation

HRID 845638 reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].[F:5][C:6]1[CH:7]=[C:8]([Br:12])[CH:9]=[CH:10][CH:11]=1.[C:13]([N:16]1[CH2:24][CH2:23][CH:19]([C:20](Cl)=[O:21])[CH2:18][CH2:17]1)(=[O:15])[CH3:14]>>[Br:12][C:8]1[CH:9]=[CH:10][C:11]([C:20]([CH:19]2[CH2:18][CH2:17][N:16]([C:13](=[O:15])[CH3:14])[CH2:24][CH2:23]2)=[O:21])=[C:6]([F:5])[CH:7]=1

Participants

4

Procedure

To a stirred suspension of 21.1 g of aluminum chloride and 63 ml of 3-fluorobromobenzene was added, portionwise, 16.0 g of 1-acetylisonipecotoyl chloride. The reaction mixture was stirred under reflux for 4 hrs. Most of the supernatant 3-fluorobromobenzene was decanted and ice water was added. The aqueous mixture was extracted with dichloromethane and the extract was washed with water, dried over anhydrous magnesium sulfate and the solvent concentrated to give an oil. The oil was triturated with ether and a solid separated out. Recrystallization of the solid from cyclohexane gave 4.9 g (19%) of product. Recrystallization from cyclohexane yielded the analytical sample, mp 111°-113° C.

Workup

  1. additionwas added
  2. temperatureunder reflux for 4 hrs
  3. customMost of the supernatant 3-fluorobromobenzene was decanted
  4. additionice water was added
  5. extractionThe aqueous mixture was extracted with dichloromethane
  6. washthe extract was washed with water
  7. dry with materialdried over anhydrous magnesium sulfate
  8. concentrationthe solvent concentrated
  9. customto give an oil
  10. customThe oil was triturated with ether
  11. customa solid separated out
  12. customRecrystallization of the solid from cyclohexane

Sources & evidence

ORD record
ord-e06a38bff15c411683f85be8141a8575
Source dataset
uspto-grants-1988_07
Patent number
US04758668

Reaction notes

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