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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322124Generated: October 26, 2026

Potassium Iodide → 4-(4,4-Diphenylpiperidin-1-yl)butyronitrile

https://huagongshe.com/reaction/322124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-BromobutyronitrileHCID 21412—
Reactant4,4-DiphenylpiperidineHCID 2823239—
Solvent1-ButanolHCID 263—
Solvent1,4-DioxaneHCID 31275—
Product4-(4,4-Diphenylpiperidin-1-yl)butyronitrileHCID 2300411687.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211198B1
Source datasetuspto-grants-2001_04
ORD IDord-f1e80845db1b4be48eefc82bf6903444
Source noteuspto-grants-2001_04