Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178524756 | HCID 178524756 | — |
| Product | HCID 68580627 | HCID 68580627 | 67% |
Reaction Steps
4-Hydroxy-2-trifluoromethyl-pyrimidine-5-carboxylic acid (1 g, 4.828 mmol, Oakwood Products) was dissolved in dimethylformamide (10 mL) and potassium carbonate (1.668 g, 12.070 mmol) was added. After stirring at room temperature for 15 min, iodoethane (0.966 mL, 12.070 mmol) was added and the reaction mixture was stirred at room temperature for 3 d. Water was added, and the product was extracted with ethyl acetate (2×). The organic layers were washed with water (1×), brine (1×) and dried over anhydrous sodium sulfate. The solids were filtered off, and the filtrate was concentrated in vacuo. Purification of the residue by flash column chromatography (silica gel, eluting with a gradient of 5-50% ethyl acetate in hexanes) to give 4-ethoxy-2-trifluoromethyl-pyrimidine-5-carboxylic acid ethyl ester (852 mg, 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07705007B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-5a5bbfc537a54bc5adf2710876657224 |
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| Source note | uspto-grants-2010_04 |
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