Acetone → 5-Bromo-3-fluorobenzene-1,2-diamine

HRID 408698Notes

Reaction equation

HRID 408698 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([F:12])[C:5]([N+:9]([O-])=O)=[C:6]([NH2:8])[CH:7]=1.[NH4+].[Cl-].CC(C)=O>[Zn].O>[Br:1][C:2]1[CH:7]=[C:6]([NH2:8])[C:5]([NH2:9])=[C:4]([F:12])[CH:3]=1

Participants

6

Conditions

Temperature
23 °C

Procedure

To a solution of 5-bromo-3-fluoro-2-nitro-phenylamine (2 g, 8.5 mmol), NH4Cl (6.81 g, 127.6 mmol), acetone (100 mL) and water (20 mL), was added zinc powder portion-wise (three equal portions over 5 minutes) (8.34 g, 127.6 mmol) at 0° C. The mixture was stirred for 2 h then warmed to 23° C. The mixture was filtered through Celite® and the solvents were concentrated under reduced pressure. The mixture was re-dissolved in EtOAc/DCM and filtered a second time through Celite® and the solvents were evaporated. The crude mixture was diluted with EtOAc (200 mL), washed with brine (40 mL), dried, filtered, and concentrated under reduced pressure. The resultant residue was used in the next reaction without further purification.

Workup

  1. filtrationThe mixture was filtered through Celite®
  2. concentrationthe solvents were concentrated under reduced pressure
  3. dissolutionThe mixture was re-dissolved in EtOAc/DCM
  4. filtrationfiltered a second time through Celite®
  5. customthe solvents were evaporated
  6. additionThe crude mixture was diluted with EtOAc (200 mL)
  7. washwashed with brine (40 mL)
  8. customdried
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure
  11. customThe resultant residue was used in the next reaction without further purification

Sources & evidence

ORD record
ord-d89cf31e572949aaab12efec56e135eb
Source dataset
uspto-grants-2014_06
Patent number
US08759345B2

Reaction notes

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