Acetone → 3-(Methylsulfonyl)benzenesulfonamide

HRID 2303577Notes

Reaction equation

HRID 2303577 reaction equation
CS[C:3]1[CH:4]=[C:5]([S:9]([NH2:12])(=[O:11])=[O:10])[CH:6]=[CH:7][CH:8]=1.OO[S:15]([O-:17])=[O:16].[K+].[CH3:19]C(C)=O>>[CH3:19][S:15]([C:7]1[CH:6]=[C:5]([S:9]([NH2:12])(=[O:11])=[O:10])[CH:4]=[CH:3][CH:8]=1)(=[O:17])=[O:16]

Participants

4

Reactant 3

HCID 180AcetoneHCID 18461638HCID 18461638, compoundHCID 23707502Potassium hydroxy sulfite

Product 1

HCID 136682473-(Methylsulfonyl)benzenesulfonamide

Procedure

To a solution of 3-methylsulfanylbenzenesulfonamide (500 mg, 2.5 mmol) in acetone was added an aqueous solution of OXONE® (3.2 grams, 5 mmol). The mixture was stirred at room temperature for 12 hours. The reaction was evaporated to dryness in vacuo. The residue was triturated with acetone and filtered. The filtrated was evaporated to give 460 mg of the titled compound.

Workup

  1. customThe reaction was evaporated to dryness in vacuo
  2. customThe residue was triturated with acetone
  3. filtrationfiltered
  4. customThe filtrated was evaporated

Sources & evidence

ORD record
ord-05a860a766c343fe91bea6b49b8dd101
Source dataset
uspto-grants-2002_08
Patent number
US06433009B1

Reaction notes

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