5-Fluoro-2-nitrophenol → 2-Amino-5-fluorophenol

HRID 334560Notes

Reaction equation

HRID 334560 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([OH:11])[C:5]([N+:8]([O-])=O)=[CH:6][CH:7]=1>C(O)(=O)C.[Zn]>[NH2:8][C:5]1[CH:6]=[CH:7][C:2]([F:1])=[CH:3][C:4]=1[OH:11]

Participants

4

Procedure

A suspension of 3-fluoro-6-nitrophenol (500 mg, 3.18 mmol) and zinc (2.10 g, 31.8 mmol) in acetic acid (7.3 mL) was stirred overnight at room temperature. The reaction mixture was filtered through celite and washed with DCM. After evaporation and distillation under vacuum (2.10−2 mbar) of the solvents, the residue was dissolved in DCM. The organic phase was washed with a saturated solution of NaHCO3 and brine, dried over MgSO4, filtered and evaporated. The crude residue was purified by flash chromatography (DCM/MeOH 99.5:0.5) to yield 177 mg (1.39 mmol, 44%) of 2-amino-5-fluorophenol as an orange solid.

Workup

  1. filtrationThe reaction mixture was filtered through celite
  2. washwashed with DCM
  3. customAfter evaporation and distillation under vacuum (2.10−2 mbar) of the solvents
  4. dissolutionthe residue was dissolved in DCM
  5. washThe organic phase was washed with a saturated solution of NaHCO3 and brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customevaporated
  9. customThe crude residue was purified by flash chromatography (DCM/MeOH 99.5:0.5)

Sources & evidence

ORD record
ord-96dba0dabba64a7cb0cde105bd09a60d
Source dataset
uspto-grants-2014_11
Patent number
US08883826B2

Reaction notes

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