Sodium Carbonate → 3-Fluoro-4-(methylsulfonyl)phenylhydrazine

HRID 497199Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 497199
[F:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[S:9]([CH3:12])(=[O:11])=[O:10])[NH2:5].[N:13]([O-])=O.[Na+].S([O-])([O-])=O.[Na+].[Na+].C([O-])([O-])=O.[Na+].[Na+]>Cl.O.[OH-].[Na+]>[F:1][C:2]1[CH:3]=[C:4]([NH:5][NH2:13])[CH:6]=[CH:7][C:8]=1[S:9]([CH3:12])(=[O:11])=[O:10]

Komponenten

8

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

To a stirred suspension of 3-fluoro-4-(methylsulfonyl)aniline (8.1 g, 42.9 mmol) in 20% aqueous HCl (27 mL) was added dropwise a solution of sodium nitrite (3 g, 43.5 mmol) in water (20 mL) at 0° C. After stirring for 1 hour, the resulting suspension was added to a solution of sodium sulfite (13.5 g, 110 mmol) in water (60 mL) and 20% aqueous NaOH (3 mL) at 0-5° C. Then the mixture was heated at 60-70° C. for 2 hours, and conc. HCl (3.5 mL) was added. The resulting mixture was heated for further 5 hours at 60° C. After cooling down to room temperature, the mixture was made basic by Na2CO3. The whole was extracted with THF (150 mL×3), the combined organic layer washed with brine (100 mL), dried over MgSO4, and concentrated in vacuo. The resulting solid was recrystallized from EtOH to give 3-fluoro-4-(methylsulfonyl)phenylhydrazine (5 g, 57% yield).

Aufarbeitung

  1. temperatureThe resulting mixture was heated for further 5 hours at 60° C
  2. temperatureAfter cooling down to room temperature
  3. extractionThe whole was extracted with THF (150 mL×3)
  4. washthe combined organic layer washed with brine (100 mL)
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customThe resulting solid was recrystallized from EtOH

Quellen und Nachweise

ORD-Eintrag
ord-d1554f3555d648bb9e49a8de5a708d3a
Quelldatensatz
uspto-grants-2005_09
Patentnummer
US06949536B2

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