Dimethylformamide → 2-Chloro-1,3-benzoxazol-6-OL

HRID 1988397Notes

Reaction equation

HRID 1988397 reaction equation
S[C:2]1[O:3][C:4]2[CH:10]=[C:9]([OH:11])[CH:8]=[CH:7][C:5]=2[N:6]=1.S(Cl)([Cl:14])=O.CN(C=O)C>>[Cl:14][C:2]1[O:3][C:4]2[CH:10]=[C:9]([OH:11])[CH:8]=[CH:7][C:5]=2[N:6]=1

Participants

4

Conditions

Temperature
80 °C

Procedure

2-Mercapto-benzoxazol-6-ol (1 eq) was dissolved in thionyl chloride (10 eq). DMF (0.6 eq) was slowly added to this solution at room temperature. The mixture was heated to 80° C. and refluxed for 15 minutes. The reaction mixture was cooled to room temperature and the solvent was removed. The resulting solid was azeotroped three times with xylenes. The solid was dissolved in a 10% solution of THF in ethyl acetate and washed once with a saturated aqueous solution of sodium bicarbonate. The organic layer was dried with anhydrous sodium sulfate, filtered, and the solvent removed. The solid was triturated with acetonitrile to yield pure product with a 68% yield. MH+=170.0.

Workup

  1. temperaturerefluxed for 15 minutes
  2. temperatureThe reaction mixture was cooled to room temperature
  3. customthe solvent was removed
  4. customThe resulting solid was azeotroped three times with xylenes
  5. dissolutionThe solid was dissolved in a 10% solution of THF in ethyl acetate
  6. washwashed once with a saturated aqueous solution of sodium bicarbonate
  7. dry with materialThe organic layer was dried with anhydrous sodium sulfate
  8. filtrationfiltered
  9. customthe solvent removed
  10. customThe solid was triturated with acetonitrile
  11. customto yield pure product with a 68% yield

Sources & evidence

ORD record
ord-452ecae7170446068dcd4720e59cd72c
Source dataset
uspto-grants-2009_06
Patent number
US07553854B2

Reaction notes

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