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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172127Generated: November 3, 2026

Sodium Methoxide → 5-Bromo-4-methoxy-6-(trifluoromethyl)pyrimidine

https://huagongshe.com/reaction/1172127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant5-Bromo-4-chloro-6-(trifluoromethyl)pyrimidineHCID 11536250—
SolventMethanolHCID 887—
Product5-Bromo-4-methoxy-6-(trifluoromethyl)pyrimidineHCID 1786289791%

Reaction Steps

16.7 ml of sodium methoxide (a 28% methanol solution, 86.4 mmoles) was added, at room temperature, to a solution of 21.5 g (82.2 mmoles) of 5-bromo-4-chloro-6-trifluoromethylpyrimidine dissolved in 100 ml of methanol. The mixture was stirred to give rise to a reaction. After confirmation of the completion of the reaction, the reaction mixture was subjected to vacuum distillation to remove the solvent contained therein. The residue was poured into water, followed by extraction with chloroform. The resulting organic layer was washed with water and an aqueous sodium chloride solution in this order and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein. The residue was washed with n-hexane to obtain 19.2 g (yield: 91.0%) of 5-bromo-4-methoxy-6-trifluoromethylpyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833939B2
Source datasetuspto-grants-2010_11
ORD IDord-17ea03595a7e48f486280e64c7f6cf97
Source noteuspto-grants-2010_11