Ammonium Hydroxide → 3-Chloro-4-fluorobenzenesulfonamide

HRID 2086691Notes

Reaction equation

HRID 2086691 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([S:9](Cl)(=[O:11])=[O:10])[CH:5]=[CH:6][C:7]=1[F:8].[OH-].[NH4+:14]>C(Cl)Cl>[Cl:1][C:2]1[CH:3]=[C:4]([S:9]([NH2:14])(=[O:11])=[O:10])[CH:5]=[CH:6][C:7]=1[F:8]

Participants

4

Reactant 2

HCID 14923Ammonium HydroxideHCID 1452223-Chloro-4-fluorobenzenesulphonyl chloride

Product 1

HCID 75098833-Chloro-4-fluorobenzenesulfonamideYield 68.2%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 3-chloro-4-fluorobenzenesulfonyl chloride (2.29 g, 10 mmol) in methylene chloride (30 mL) was added 25% ammonium hydroxide (10 mL) at room temperature and the mixture was stirred for 1 hour. The solvent was removed in vacuo. The residue was redissolved in ethyl acetate (50 mL) and the whole washed with water and brine. After dried over MgSO4 and concentration in vacuo. The resulting solid was recrystallized from ether-hexane to give the title compound (1.429 g, 68.2% yield).

Workup

  1. customThe solvent was removed in vacuo
  2. dissolutionThe residue was redissolved in ethyl acetate (50 mL)
  3. washthe whole washed with water and brine
  4. dry with materialAfter dried over MgSO4 and concentration in vacuo
  5. customThe resulting solid was recrystallized from ether-hexane

Sources & evidence

ORD record
ord-3d2c8b526bb641ef920c8c1943b20a4f
Source dataset
uspto-grants-2004_04
Patent number
US06727238B2

Reaction notes

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