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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859444Generated: November 2, 2026

Sodium Iodide → (S)-3-(4-Nitrobenzoyloxy)-1-(4-methoxyphenethyl)pyrrolidine

https://huagongshe.com/reaction/1859444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
Reactant2-(4-Methoxyphenyl)ethyl 4-methylbenzenesulfonateHCID 285384—
Reactant(S)-3-(4-nitrobenzoyloxy)pyrrolidineHCID 12148704—
SolventAcetonitrileHCID 6342—
Product(S)-3-(4-Nitrobenzoyloxy)-1-(4-methoxyphenethyl)pyrrolidineHCID 69901303—

Reaction Conditions

Temperature90 °C

Reaction Steps

4-Methoxyphenethyl tosylate (1.24 g, 4.05 mmol), sodium carbonate (430 mg, 4.06 mmol) and sodium iodide (40 mg, 0.26 mmol) were added to a solution of (S)-3-(4-nitrobenzoyloxy)pyrrolidine (799 mg, 3.38 mmol) in acetonitrile (40 ml), and they were heated under reflux at 90° C. for 3 hours. The insoluble material was removed by the filtration. The insoluble material was washed with ethyl acetate, and the wash solution was combined with the filtrate. The solvent was evaporated under reduced pressure. The obtained residue was subjected to silica gel column chromatography. The product was eluted with hexane and ethyl acetate (10:1) and then with a mixture of the same solvents (1:1). The appropriate fractions were combined, and the solvent was evaporated under reduced pressure to obtain (S)-3-(4-nitrobenzoyloxy)-1-(4-methoxy-phenethyl)pyrrolidine in the form of a light yellow oil (1.00 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528504B2
Source datasetuspto-grants-2003_03
ORD IDord-aaf43faa9e074a3eba372d6a44c7e83b
Source noteuspto-grants-2003_03