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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215642Generated: October 25, 2026

Sodium Iodide → n-[1-(p-Nitrophenethyl)-4-piperidinyl]-n-phenylpropionamide

https://huagongshe.com/reaction/2215642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Nitrophenethyl bromideHCID 79266—
Reactant4-(N-Propionylaniline)piperidineHCID 259381—
SolventMethyl Isobutyl KetoneHCID 7909—
Productn-[1-(p-Nitrophenethyl)-4-piperidinyl]-n-phenylpropionamideHCID 1340892356%

Reaction Steps

A suspension of norfentanyl of Example 4 (6.71 g, 0.029 mol), p-nitrophenethylbromide (7.178 g, 0.0372 mol), potassium carbonate (19 g, 0.14 mol) and a few crystals of sodium iodide in 4-methyl-2-pentanone (200 ml) was stirred overnight at reflux, under nitrogen. After cooling to room temperature, the precipitate was removed by filtration and the solution concentrated under reduced pressure. The dark residue was dissolved in ethyl acetate (200 ml) and washed with water (2×100 ml), dried over sodium sulfate, filtered and the solvent removed in vacuo. The residue was purified by column chromatography (silica gel, 10% MeOH/90% CHCl3 v/v) to give the title compound as a yellow solid (5.33 g, 56% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109310B2
Source datasetuspto-grants-2006_09
ORD IDord-f5ba4c2185494aaba25de8ea0744f985
Source noteuspto-grants-2006_09