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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 5-Bromo-4-methoxy-6-(trifluoromethyl)pyrimidine | HCID 17862897 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methoxy-6-trifluoromethyl-pyrimidine-5-carbaldehyde | HCID 17862898 | 15.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07238689B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-4c96c9afe7704d26b9eac05631e0f9ff |
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| Source note | uspto-grants-2007_07 |
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