HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485108Generated: November 2, 2026
Water → [1-(Pyrimidin-2-yl)piperidin-4-yl]methanol
https://huagongshe.com/reaction/1485108
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Reactant | 4-Piperidinemethanol | HCID 420771 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [1-(Pyrimidin-2-yl)piperidin-4-yl]methanol | HCID 2776521 | 89.4% |
Reaction Steps
To a solution of 4-piperidinemethanol (1.00 g) in dimethyl sulfoxide (28.9 mL), 2-chloropyrimidine (994 mg) and potassium carbonate (2.40 g) were added and the mixture was stirred at 100° C. for three hours. After cooling the reaction mixture to room temperature, water was added to it and extraction was conducted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and after removing the desiccant by filtration, the filtrate was concentrated under reduced pressure to give [1-([pyrimidin-2-yl)piperidin-4-yl]methanol as a colorless oil (1.50 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422240B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-a1999d9a8d8c4eabbe8845792a9825cc |
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| Source note | uspto-grants-2016_08 |
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