HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527643Generated: November 1, 2026
Acetone → 5-Ethylpyrimidine-4-carboxylic acid
https://huagongshe.com/reaction/1527643
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Ethyl-4-(furan-2-yl)-pyrimidine | HCID 67810695 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Ethylpyrimidine-4-carboxylic acid | HCID 67812084 | — |
Reaction Steps
A mixture of 5-ethyl-4-(furan-2-yl)-pyrimidine (2.03 g), acetone (70 ml), and water (35 ml) was stirred at 50° C., potassium permanganate (15 g) was added thereto over 15 minutes, and the reaction mixture was stirred under reflux for 1 hour. After standing to cool the reaction mixture to room temperature, to the reaction mixture, saturated aqueous sodium hydrogen carbonate solution was added, and extracted with tert-butyl methyl ether. To the resulting aqueous layer, hydrochloric acid was added, and extracted with tert-butyl methyl ether. The organic layer was dried over sodium sulfate, and concentrated under reduced pressure to give 1.14 g of 5-ethyl-pyrimidine-4-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09089136B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-753da51736544f89aa051f4cf5c42177 |
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| Source note | uspto-grants-2015_07 |
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