Sulfuric Acid → 1,2-Benzothiazol-5-ol

HRID 252149Notes

Reaction equation

HRID 252149 reaction equation
N[C:2]1[CH:3]=[CH:4][C:5]2[S:9][N:8]=[CH:7][C:6]=2[CH:10]=1.S(=O)(=O)(O)[OH:12].N([O-])=O.[Na+]>O>[S:9]1[C:5]2[CH:4]=[CH:3][C:2]([OH:12])=[CH:10][C:6]=2[CH:7]=[N:8]1

Participants

5

Conditions

Temperature
90 °C

Procedure

5-Aminobenzo[d]isothiazole (217 mg, 1.45 mmol) was suspended/dissolved in water (20 mL) containing concentrated sulphuric acid (1.5 mL) and heated at 90° C. for 2 h. This solution was cooled to 0° C. and sodium nitrite (105 mg, 1.52 mmol) in water (1 mL) was added over 5 min and the mixture allowed to warm to ambient temperature. The diazonium salt was added dropwise over 20 min to a solution of concentrated sulphuric acid (1 mL) in water (12 mL) at 90° C. and stirred at this temperature for 2 h before hot filtering to remove an insoluble solid. The filtrate was extracted with dichloromethane (3×20 mL) and the combined organic extracts washed with brine (50 mL), dried (MgSO4) and concentrated in vacuo to give the title compound as a brown solid (65 mg, 30%).

Workup

  1. temperatureThis solution was cooled to 0° C.
  2. temperatureto warm to ambient temperature
  3. filtrationbefore hot filtering
  4. customto remove an insoluble solid
  5. extractionThe filtrate was extracted with dichloromethane (3×20 mL)
  6. washthe combined organic extracts washed with brine (50 mL)
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-10dccd6e2a7f4de382b4276eb5c8f13e
Source dataset
uspto-grants-2011_01
Patent number
US07868017B2

Reaction notes

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