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3-Fluoro-4-nitrophenol → 4-Amino-3-fluorophenol

HRID 520693
Notes
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Reaction equation

HRID 520693 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([OH:11])[CH:5]=[CH:6][C:7]=1[N+:8]([O-])=O.C(O[K])=O>C1COCC1.O.[Pd]>[NH2:8][C:7]1[CH:6]=[CH:5][C:4]([OH:11])=[CH:3][C:2]=1[F:1]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 5209483-Fluoro-4-nitrophenolHCID 178526052HCID 178526052, compound

Product 1

HCID 27359194-Amino-3-fluorophenolYield 72.3%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 21881883Oxolane--water (1/1)Solvent

Conditions

Temperature
50 °C
On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Procedure

A suspension of 3-fluoro-4-nitrophenol (2.0 g, 12.73 mmol), 10% Pd/C (0.4 g) and HCOOK (8.75 g, 101.85 mmol) in THF/H2O (70 mL/20 mL) was stirred at 50° C. for 5 hours, then cooled to rt, and filtered through CELITE®. The filtrate was diluted with water (30 mL) and extracted with THF (50 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was diluted with water (50 mL) and extracted with DCM (50 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo to give the title compound as a brown solid (1.17 g, 72.3%).

Workup

  1. temperaturecooled to rt
  2. filtrationfiltered through CELITE®
  3. additionThe filtrate was diluted with water (30 mL)
  4. extractionextracted with THF (50 mL)
  5. dry with materialThe organic layer was dried over Na2SO4
  6. concentrationconcentrated in vacuo
  7. additionThe residue was diluted with water (50 mL)
  8. extractionextracted with DCM (50 mL)
  9. dry with materialThe organic layer was dried over anhydrous Na2SO4
  10. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-ce6b1edf87cc4a6695d4e06fe3070df3
Source dataset
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09326975B2

Reaction notes

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