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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292822Generated: October 30, 2026

Ethyl formate → 4-Methoxy-6-trifluoromethyl-pyrimidine-5-carbaldehyde

https://huagongshe.com/reaction/1292822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl formateHCID 8025—
ReactantHexaneHCID 8058—
Reactant5-Bromo-4-methoxy-6-(trifluoromethyl)pyrimidineHCID 17862897—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Methoxy-6-trifluoromethyl-pyrimidine-5-carbaldehydeHCID 1786289815.8%

Reaction Steps

30.0 ml of n-butyllithium (a 1.6 moles/liter n-hexane solution, 48.0 mmoles) was gradually added, at −65 to −60° C., to a solution of 10.3 g (40.0 mmoles) of 5-bromo-4-methoxy-6-trifluoromethylpyrimidine dissolved in 100 ml of tetrahydrofuran. The mixture was stirred for 30 minutes. Thereto was added 3.6 g (48.0 mmoles) of ethyl formate at the same temperature. The resulting mixture was stirred at the same temperature for 3 hours to give rise to a reaction. The reaction mixture was poured into water, followed by extraction with ethyl acetate. 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 1.3 g (yield: 15.8%) of 4-methoxy-6-trifluoromethylpyrimidine-5-carboaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238689B2
Source datasetuspto-grants-2007_07
ORD IDord-4c96c9afe7704d26b9eac05631e0f9ff
Source noteuspto-grants-2007_07