HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180163Generated: October 30, 2026
Potassium Carbonate → 4-(4-Iodo-phenyl)-1-(3,3,3-trifluoro-propyl)-piperidine-4-carbonitrile
https://huagongshe.com/reaction/2180163
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromo-1,1,1-trifluoropropane | HCID 2725114 | — |
| Reactant | 4-(4-Iodo-phenyl)-piperidine-4-carbonitrile | HCID 22490372 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(4-Iodo-phenyl)-1-(3,3,3-trifluoro-propyl)-piperidine-4-carbonitrile | HCID 22490343 | 98% |
Reaction Steps
To a solution of the crude 4-(4-iodo-phenyl)-piperidine-4-carbonitrile (0.60 g, ˜1.9 mmol) in CH3CN (6 mL) was added (3,3,3-trifluoro)-propyl bromide (1.02 mL, 9.6 mmol, 5 eq.) and K2CO3 (1.33 g, 9.6 mmol, 5 eq.) and the resulting mixture was stirred and heated to 60° C. for 16 h. The reaction was cooled to room temperature, diluted with EtOAc (20 mL) and washed with H2O (25 mL) and saturated brine (2×25 mL). The organic phase was dried over anhydrous Na2SO4, filtered and concentrated by rotary evaporation to give the crude 4-(4-iodo-phenyl)-1-(3,3,3-trifluoro-propyl)-piperidine-4-carbonitrile as a red solid (0.761 g, 1.86 mmol, 98%). 1H NMR (300 MHz, CDCl3): δ 7.83 (dd, 2H), 7.33 (dd, 2H), 3.09 (d, 2H), 2.82 (dd, 2H), 2.66 (td, 2H), 2.45 (m, 2H), 2.18 (m, 4H); MS (ESI): 409.1/410.2 (M +1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06887889B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-d558c4cb85864afbaf4583a1e036ba4a |
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| Source note | uspto-grants-2005_05 |
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