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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461728Generated: November 1, 2026

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

https://huagongshe.com/reaction/1461728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
Reactant4-Hydroxy-6-(trifluoromethyl)pyrimidineHCID 135458620—
SolventAcetic AcidHCID 176—
Product5-Bromo-6-(trifluoromethyl)pyrimidin-4-olHCID 13542460075.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

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.);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05077297
Source datasetuspto-grants-1991_12
ORD IDord-b6973b3552164b1c9ed4fb650f225849
Source noteuspto-grants-1991_12