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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396617Generated: October 30, 2026

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

https://huagongshe.com/reaction/396617

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 numberUS06608086B2
Source datasetuspto-grants-2003_08
ORD IDord-a4f3de259dc745fa8bcd847bf83bd139
Source noteuspto-grants-2003_08