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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254221Generated: October 26, 2026

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

https://huagongshe.com/reaction/254221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhosphorus tribromideHCID 24614—
Reactant(4-Ethoxy-6-trifluoromethylpyrimidin-5-yl)-methanolHCID 17862901—
SolventMethanolHCID 887—
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 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 in methanol and the solution was stirred for 1 hour to give rise to a reaction. The reaction mixture was poured into water and extraction with ether was conducted. 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 reduced pressure distillation to remove the solvent contained therein, to obtain a crude product of 5-bromomethyl-4-ethoxy-6-trifluoromethylpyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875606B2
Source datasetuspto-grants-2011_01
ORD IDord-175b5ee55b8e4b03915ba128de3ac962
Source noteuspto-grants-2011_01