Sodium Carbonate → 3-Fluoro-4-(methylsulfonyl)phenylhydrazine
Reaction equation
[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]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Conditions
- Temperature
- 65 °C
Procedure
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).
Workup
- temperatureThe resulting mixture was heated for further 5 hours at 60° C
- temperatureAfter cooling down to room temperature
- extractionThe whole was extracted with THF (150 mL×3)
- washthe combined organic layer washed with brine (100 mL)
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
- customThe resulting solid was recrystallized from EtOH
Sources & evidence
- ORD record
- ord-d1554f3555d648bb9e49a8de5a708d3a
- Source dataset
- uspto-grants-2005_09
- Patent number
- US06949536B2
Reaction notes
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