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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | (4-Ethoxy-6-trifluoromethylpyrimidin-5-yl)-methanol | HCID 17862901 | — |
| Solvent | Methanol | HCID 887 | — |
| 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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875606B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-175b5ee55b8e4b03915ba128de3ac962 |
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| Source note | uspto-grants-2011_01 |
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