Ethanol → 4-Bromo-3-fluorobenzene-1,2-diamine

HRID 1053895Notes

Reaction equation

HRID 1053895 reaction equation
[Br:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([N+:9]([O-])=O)[C:3]=1[F:12].CCO.O.[Cl-].[NH4+]>C1COCC1.[Fe]>[Br:1][C:2]1[C:3]([F:12])=[C:4]([NH2:9])[C:5]([NH2:6])=[CH:7][CH:8]=1

Participants

7

Conditions

Temperature
80 °C

Procedure

To a solution of 4-bromo-3-fluoro-2-nitroaniline (3.0 g, 12.8 mmol) in THF (30 mL) was added EtOH (30 mL) and H2O (10 mL) followed by iron powder (3.6 g, 63.8 mmol) and ammonium chloride (1.0 g, 19.2 mmol). The resulting mixture was stirred at 80° C. for 16 hours. The mixture was cooled to room temperature and filtered through diatomaceous earth. The solid was washed with EtOH until no further color came through the filter. The filtrate was concentrated in vacuo and the crude product was purified by column chromatography on silica gel using a solvent gradient of 0-40% EtOAc in hexane to give the title compound (2.2 g, 84%).

Workup

  1. temperatureThe mixture was cooled to room temperature
  2. filtrationfiltered through diatomaceous earth
  3. washThe solid was washed with EtOH until no further color
  4. concentrationThe filtrate was concentrated in vacuo
  5. customthe crude product was purified by column chromatography on silica gel using a solvent gradient of 0-40% EtOAc in hexane

Sources & evidence

ORD record
ord-9307c6a08fa6448c83093686af8325cf
Source dataset
uspto-grants-2016_07
Patent number
US09394279B2

Reaction notes

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