Hydrogen Peroxide → HCID 18697495, compound

HRID 2289400Notes

Reaction equation

HRID 2289400 reaction equation
[CH3:1][C:2]1([CH3:11])[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[Se:4][NH:3]1.[OH:12]O>CO>[CH3:1][C:2]1([CH3:11])[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[Se:4](=[O:12])[NH:3]1

Participants

4

Procedure

The derivative 3,3-dimethyl-benzisoselenazoline BXT-51056 (212 mg; 1 mmole) was dissolved at room temperature in methanol (5 ml) with stirring. After addition of 5% hydrogen peroxide (600 μl; 1.05 mmole), stirring was continued for 15 min. The solvent was evaporated off under reduced pressure. The residue was taken up in 25 ml of dichloromethane and washed with 3×3 ml of a saturated NaCl solution, dried over Na2SO4 then filtered. After evaporation of the solvent under reduced pressure, the desired product was obtained in the form of yellowish crystals.

Workup

  1. stirringstirring
  2. customThe solvent was evaporated off under reduced pressure
  3. washwashed with 3×3 ml of a saturated NaCl solution
  4. dry with materialdried over Na2SO4
  5. filtrationthen filtered
  6. customAfter evaporation of the solvent under reduced pressure

Sources & evidence

ORD record
ord-aa15ec8b5cc449d39358cff0768b10f7
Source dataset
uspto-grants-2000_07
Patent number
US06093532

Reaction notes

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