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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172128Generated: November 3, 2026

Sodium ethoxide → 5-Bromo-4-ethoxy-6-trifluoromethylpyrimidine

https://huagongshe.com/reaction/1172128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
Reactant5-Bromo-4-chloro-6-(trifluoromethyl)pyrimidineHCID 11536250—
SolventEthanolHCID 702—
Product5-Bromo-4-ethoxy-6-trifluoromethylpyrimidineHCID 1786287782.9%

Reaction Steps

0.94 g (13.77 mmoles) of sodium ethoxide was added, at room temperature, to a solution of 3.00 g (11.48 mmoles) of 5-bromo-4-chloro-6-trifluoromethylpyrimidine dissolved in 50 ml of ethanol. 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 purified by silica gel column chromatography to obtain 2.44 g (yield: 82.9%) of 5-bromo-4-ethoxy-6-trifluoromethylpyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833939B2
Source datasetuspto-grants-2010_11
ORD IDord-f3d6531967b447a2b4f512e6254f84c7
Source noteuspto-grants-2010_11