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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396620Generated: October 30, 2026

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

https://huagongshe.com/reaction/396620

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 numberUS06608086B2
Source datasetuspto-grants-2003_08
ORD IDord-d61701e4ab974ff4904e8431c928817a
Source noteuspto-grants-2003_08