HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → (4,4-Diphenylpiperidin-1-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,4-Diphenylpiperidine | HCID 2823239 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (4,4-Diphenylpiperidin-1-yl)acetonitrile | HCID 23004060 | 86% |
Reaction Steps
A suspension of 4,4-diphenylpiperidine (4.00 g, 16.9 mmol, 1.00 equiv), chloroacetonitrile (1.40 mL, 21.9 mmol, 1.30 equiv, Aldrich), potassium carbonate (4.67 g, 33.8 mmol, 2.00 equiv), and potassium iodide (561 mg, 3.38 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. The residue was purified by flash chromatography (SiO2, EtoAc) to afford 4.01 g (86%) of white solid, which was characterized spectroscopically.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06310076B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-4e6dd4ca86b941c58ed01f7d2ea83129 |
| Source note | uspto-grants-2001_10 |