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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364209Generated: October 25, 2026

Sodium Iodide → (2R)-1-[3-(4-iodophenoxy)propyl]-2-methylpyrrolidine

https://huagongshe.com/reaction/1364209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-2-MethylpyrrolidineHCID 641544—
Reactant1-(3-Chloropropoxy)-4-iodobenzeneHCID 15895520—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product(2R)-1-[3-(4-iodophenoxy)propyl]-2-methylpyrrolidineHCID 57675747—

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 1-(3-chloropropoxy)-4-iodobenzene obtained in Example 1-(1) (2.79 g), (R)-2-methylpyrrolidine (0.961 g), sodium iodide (0.282 g) and potassium carbonate (2.60 g) in acetonitrile (2.8 mL) was stirred in a sealed tube at 100° C. for 5 hours. The reaction mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate. The organic layer was washed with water and brine, dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluting solvent: n-hexane:ethyl acetate=10:1) to give the titled compound (3.27 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888354B2
Source datasetuspto-grants-2011_02
ORD IDord-da6da89c92d94b1c82d0d10ea9197d78
Source noteuspto-grants-2011_02