HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278918Generated: October 25, 2026
Potassium Iodide → 3-(4-Cyano-4-phenylpiperidin-1-yl)propylphthalimide
https://huagongshe.com/reaction/278918
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Phenylpiperidine-4-carbonitrile hydrochloride | HCID 3084973 | — |
| Reactant | Bromopropylphthalimide | HCID 21958088 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4-Cyano-4-phenylpiperidin-1-yl)propylphthalimide | HCID 22725223 | — |
Reaction Steps
A mixture of 4-cyano-4-phenylpiperidine hydrochloride (111 g, 0.5 mol), 3-bromopropylphthalimide (135.39 g, 0.505 mol), potassium carbonate (276.42 g, 2 mol), and potassium iodide (5.4 g) in DMF (1 L) was stirred and heated at 100-110° C. for 8 hours. About 80% of the solvent was evaporated at reduced pressure, the residue was diluted with dichloromethane (1 L) and washed with brine (3×300 mL) and dried (Na2SO4). Solvent was evaporated from the dichloromethane solution and the residue was treated with isopropanol (400 mL) and cooled. The pale yellow crystalline product formed was filtered, washed with ice-cold isopropanol and dried (168.6 g, 90%); M.p. 96-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06362182B1 |
|---|
| Source dataset | uspto-grants-2002_03 |
|---|
| ORD ID | ord-580537028e0e433ca7b4df9366a19cd3 |
|---|
| Source note | uspto-grants-2002_03 |
|---|