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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172134Generated: October 26, 2026

Methanol → 5-Bromomethyl-4-ethoxy-6-trifluoromethylpyrimidine

https://huagongshe.com/reaction/1172134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantPhosphorus tribromideHCID 24614—
Reactant(4-Ethoxy-6-trifluoromethylpyrimidin-5-yl)-methanolHCID 17862901—
SolventDiethyl EtherHCID 3283—
Product5-Bromomethyl-4-ethoxy-6-trifluoromethylpyrimidineHCID 17862857—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3.77 g (17.0 mmoles) of (4-ethoxy-6-trifluoromethylpyrimidin-5-yl)-methanol dissolved in 50 ml of diethyl ether was cooled to 0° C. Thereto was added 2.0 g (7.2 mmoles) of phosphorus tribromide. The mixture was stirred at room temperature for 1 hour. The resulting salt was dissolved using methanol. The resulting mixture was stirred for 1 hour to give rise to a reaction. The reaction mixture was poured into water, followed by extraction with diethyl ether. The resulting organic layer was washed with an aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein, to obtain crude 5-bromomethyl-4-ethoxy-6-trifluoromethylpyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833939B2
Source datasetuspto-grants-2010_11
ORD IDord-2f419be3589441148fa331254a205b4d
Source noteuspto-grants-2010_11