Sulfuric Acid → 3-Amino-4-fluorophenol

HRID 2266560Notes

Reaction equation

HRID 2266560 reaction equation
N([O-])=O.[Na+].N[C:6]1[CH:7]=[CH:8][C:9]([F:16])=[C:10]([NH:12]C(=O)C)[CH:11]=1.S(=O)(=O)(O)[OH:18].NC(N)=O.[OH-].[Na+]>O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Cu+2]>[NH2:12][C:10]1[CH:11]=[C:6]([OH:18])[CH:7]=[CH:8][C:9]=1[F:16]

Participants

8

Conditions

Temperature
5 °C

Procedure

A solution of sodium nitrite (17.3 g) in water (40 mL) was added dropwise to a mixture of N-(5-amino-2-fluorophenyl)acetamide (36.7 g), sulfuric acid (50 mL) and water (270 mL) at 0-10° C. The mixture was stirred at 0-10° C. for 20 minutes and then a solution of urea (2.0 g) in water (20 mL) was added and the resulting mixture stirred at 0-10° C. for a further 20 minutes. The mixture was added dropwise over a period 75 minutes to a stirred solution of copper sulfate pentahydrate (131 g) in water (110 mL) at 130° C. and the resulting mixture heated at 130° C. for 2.5 hours. The mixture was cooled in an ice bath and the pH of the solution adjusted to 14 by the addition of 30% aqueous sodium hydroxide solution. The mixture was filtered through hyflo, washing with water. The pH of the filtrate was acidified by the addition of concentrated hydrochloric acid and extracted with ethyl acetate. The combined extracts were dried over magnesium sulfate and the solvent removed under reduced pressure to afford title compound as a brown solid, 22.1 g.

Workup

  1. stirringthe resulting mixture stirred at 0-10° C. for a further 20 minutes
  2. temperaturethe resulting mixture heated at 130° C. for 2.5 hours
  3. temperatureThe mixture was cooled in an ice bath
  4. filtrationThe mixture was filtered through hyflo
  5. washwashing with water
  6. additionThe pH of the filtrate was acidified by the addition of concentrated hydrochloric acid
  7. extractionextracted with ethyl acetate
  8. dry with materialThe combined extracts were dried over magnesium sulfate
  9. customthe solvent removed under reduced pressure

Sources & evidence

ORD record
ord-91fb0037b6b24ed581ae5d864c7f6cad
Source dataset
uspto-grants-2010_12
Patent number
US07858640B2

Reaction notes

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