HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878941Generated: October 27, 2026
Water → 4-[2-Fluoro-3-(methylsulfonyl)phenyl]-1-propylpiperidine
https://huagongshe.com/reaction/1878941
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | 4-[2-Fluoro-3-(methylsulfonyl)phenyl]piperidine | HCID 57448038 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-[2-Fluoro-3-(methylsulfonyl)phenyl]-1-propylpiperidine | HCID 11514933 | 79.7% |
Reaction Steps
To a solution of 4-[2-fluoro-3-(methylsulfonyl)phenyl]piperidine (0.4 g, 1.55 mmol) in acetonitrile (40 ml) was added potassium carbonate (0.3 g, 2.17 mmol) and 1-iodopropane (0.151 ml, 1.55 mmol) and the mixture was heated at reflux for 15 h. The mixture was cooled to ambient temperature and water (50 ml) was added. The aqueous residue was extracted with ethylacetate (3×50 ml) and the combined organic phases was dried, concentrated, and purified by flash column chromatography (ethylacetate/methanol, 1:1) to give the title compound (0.37 g, 79%). The amine was converted to the hydrochloric acid salt and recrystallized from ethanol/diethyl ether: M.p. 255-257° C. MS m/z (relative intensity, 70 eV) 299 (M+, 2), 271 (16), 270 (bp), 147 (9) 133 (10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314126B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-e4440f9b7aa0407286abe311330d70de |
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| Source note | uspto-grants-2012_11 |
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