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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826232Generated: October 27, 2026

Potassium Iodide → 4-(1-Benzylpiperidin-4-ylidenemethyl)benzamide

https://huagongshe.com/reaction/1826232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantTriethyl phosphiteHCID 31215—
Reactant4-(Chloromethyl)benzamideHCID 458363—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product4-(1-Benzylpiperidin-4-ylidenemethyl)benzamideHCID 992257485.9%

Reaction Steps

The compound (25.0 g, 0.147 mol) obtained in Example 1, triethyl phosphite (29.4 g, 0.177 mol), potassium iodide (22.0 g, 0.133 mol) and acetonitrile (125 mL) were charged and stirred under reflux for 3 hrs. The reaction mixture was allowed to return to room temperature, and concentrated under reduced pressure. To the residue were added N,N-dimethylformamide (100 mL) and 1-benzyl-4-piperidone (30.6 g, 0.162 mol), and the mixture was stirred under ice-cooling. Potassium t-butoxide (23.1 g, 0.206 mol) was added in 3 portions at 15 min. intervals. The reaction mixture was stirred at room temperature for 45 min. Water (400 mL) was dropwise added under ice-cooling, and the mixture was stirred for 30 min. Crystals were collected by filtration, washed with cold water (180 mL) and dried in vacuo at 40° C. to give the title compound (38.7 g, yield 85.2%) as pale-yellow powdery crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049441B2
Source datasetuspto-grants-2006_05
ORD IDord-93846d2879024d4290f375ecfaa82b59
Source noteuspto-grants-2006_05