HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693081Generated: November 5, 2026
Dimethyl Sulfoxide → 5-bromo-1-ethyl-1H-pyrimidin-2-one
https://huagongshe.com/reaction/1693081
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178419744 | HCID 178419744 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-bromo-1-ethyl-1H-pyrimidin-2-one | HCID 67281934 | 60.3% |
Reaction Steps
With cooling with ice, potassium carbonate (13.2 g, 95.7 mmol) and ethyl iodide (2.84 mL, 35.6 mmol) were added to a dimethyl sulfoxide (130 mL) solution of 5-bromo-2-hydroxypyrimidine hydrobromide (7.0 g, 27.3 mmol), and stirred at 15° C. for 16 hours. Water was added to the reaction mixture, and extracted three times with ethyl acetate. The organic layer was washed with saturated brine, dried with anhydrous sodium sulfate and then concentrated under reduced pressure. The organic layer was washed with saturated brine, dried with anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified through silica gel column chromatography (C-300, hexane/ethyl acetate=1/1) to obtain the entitled compound (3.34 g, 60%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158652B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-a0b9003a24f14d40b79f5c9cd6e9718f |
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| Source note | uspto-grants-2012_04 |
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