Potassium Nitrate → 3,3-Dimethyl-6-nitro-2,3-dihydro-benzo[d]isothiazole 1,1-dioxide

HRID 1786351Notes

Reaction equation

HRID 1786351 reaction equation
[CH3:1][C:2]1([CH3:13])[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[S:4](=[O:12])(=[O:11])[NH:3]1.[N+:14]([O-])([O-:16])=[O:15].[K+]>OS(O)(=O)=O>[CH3:1][C:2]1([CH3:13])[C:6]2[CH:7]=[CH:8][C:9]([N+:14]([O-:16])=[O:15])=[CH:10][C:5]=2[S:4](=[O:12])(=[O:11])[NH:3]1

Participants

4

Reactant 2

HCID 24434Potassium NitrateHCID 44473552,3-Dihydro-3,3-dimethyl-1,2-benzisothiazole 1,1-dioxide

Product 1

HCID 222493723,3-Dimethyl-6-nitro-2,3-dihydro-benzo[d]isothiazole 1,1-dioxide

Reagents, catalysts & solvents 1

HCID 1118Sulfuric AcidSolvent

Conditions

Temperature
0 °C

Procedure

3,3-Dimethyl-2,3-dihydro-benzo[d]isothiazole 1,1-dioxide was added to KNO3 in H2SO4 cooled to 0° C. and stirred for 15 min. The reaction was warmed to RT and stirred overnight. The mix was poured into ice and extracted with EtOAc (3×), washed with H2O and brine, dried and evaporated to give the compound which was used without further purification.

Workup

  1. temperatureThe reaction was warmed to RT
  2. stirringstirred overnight
  3. additionThe mix was poured into ice
  4. extractionextracted with EtOAc (3×)
  5. washwashed with H2O and brine
  6. customdried
  7. customevaporated
  8. customto give the compound which
  9. customwas used without further purification

Sources & evidence

ORD record
ord-a4cbbdc887974a06bd7b11a541cdc418
Source dataset
uspto-grants-2009_03
Patent number
US07507748B2

Reaction notes

Loading…