Bromine → 5-Bromo-6-(trifluoromethyl)pyrimidin-4-ol

HRID 1461728Notes

Reaction equation

HRID 1461728 reaction equation
[Br:1]Br.[F:3][C:4]([F:13])([F:12])[C:5]1[N:6]=[CH:7][NH:8][C:9](=[O:11])[CH:10]=1.C([O-])(=O)C.[Na+]>C(O)(=O)C>[Br:1][C:10]1[C:9](=[O:11])[NH:8][CH:7]=[N:6][C:5]=1[C:4]([F:3])([F:12])[F:13]

Participants

5

Conditions

Temperature
80 °C

Procedure

Bromine (4.62 g) was added in one portion to a stirred solution of 4-trifluoromethylpyrimidin-6-one (4.3 g) and sodium acetate (10.53 g) in acetic acid (43 ml). After stirring for 2 hours, the reaction mixture was left to stand for a period of 3 days, after which time it was heated to 80° C. for 1 hour. After cooling to the ambient temperature (ca 22° C.), the solvent was evaporated under reduced pressure. The resultant orange solid was dissolved in ethyl acetate, and washed several times with water. The combined agueous washings were extracted with ethylacetate, and the combined organic layers were washed with agueous sodium thiosulphate solution, followed by agueous sodium bicarbonate solution and brine. After drying over magnesium sulphate, evaporation of the solvent under reduced pressure gave 5-bromo-4-trifluoromethylpyrimidin-6-one as a white solid (4.8 g, mpt 226°-227° C.);

Workup

  1. waitthe reaction mixture was left
  2. waitto stand for a period of 3 days
  3. temperatureAfter cooling to the ambient temperature (ca 22° C.)
  4. customthe solvent was evaporated under reduced pressure
  5. dissolutionThe resultant orange solid was dissolved in ethyl acetate
  6. washwashed several times with water
  7. extractionThe combined agueous washings were extracted with ethylacetate
  8. washthe combined organic layers were washed with agueous sodium thiosulphate solution
  9. dry with materialAfter drying over magnesium sulphate, evaporation of the solvent under reduced pressure

Sources & evidence

ORD record
ord-b6973b3552164b1c9ed4fb650f225849
Source dataset
uspto-grants-1991_12
Patent number
US05077297

Reaction notes

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