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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | (4-Ethoxy-6-trifluoromethylpyrimidin-5-yl)-methanol | HCID 17862901 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-Bromomethyl-4-ethoxy-6-trifluoromethylpyrimidine | HCID 17862857 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07833939B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-2f419be3589441148fa331254a205b4d |
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| Source note | uspto-grants-2010_11 |
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