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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322121Generated: October 26, 2026

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

https://huagongshe.com/reaction/322121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantChloroacetonitrileHCID 7856—
ReactantPotassium CarbonateHCID 11430—
Reactant4,4-DiphenylpiperidineHCID 2823239—
Solvent1-ButanolHCID 263—
Solvent1,4-DioxaneHCID 31275—
Product(4,4-Diphenylpiperidin-1-yl)acetonitrileHCID 2300406086%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211198B1
Source datasetuspto-grants-2001_04
ORD IDord-54fe06006a004a049e0ed3324f22f233
Source noteuspto-grants-2001_04