HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 4-(4,4-Diphenylpiperidin-1-yl)butyronitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Reactant | 4,4-Diphenylpiperidine | HCID 2823239 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(4,4-Diphenylpiperidin-1-yl)butyronitrile | HCID 23004116 | 87.3% |
Reaction Steps
A suspension of 4,4-diphenylpiperidine (4.15 g, 17.5 mmol, 1.00 equiv), 4-bromobutyronitrile (2.10 mL, 21.0 mmol, 1.20 equiv, Aldrich), potassium carbonate (4.85 g, 35.0 mmol, 2.00 equiv), and potassium iodide (581 mg, 3.50 mmol, 0.20 equiv) in n-butanol (20 mL) and 1,4-dioxane (20 mL) was stirred at reflux under argon for 48 hours. The mixture was cooled to room temperature and concentrated. Water (50 mL) was added and the mixture was extracted with CH2Cl2 (4×150 mL) . The combined organic solutions were dried over MgSO4 and concentrated. The residue was purified by flash chromatography (SiO2, EtOAc) to afford 4.65 g (87%) of white solid, which was characterized spectroscopically.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211198B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-f1e80845db1b4be48eefc82bf6903444 |
| Source note | uspto-grants-2001_04 |