Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032337Generated: November 1, 2026

Potassium Iodide → 1-[3-(Diphenylmethoxy)propyl] 3-(3-methoxyphenyl)pyrrolidine

https://huagongshe.com/reaction/1032337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(3-Methoxyphenyl)pyrrolidineHCID 12937991—
Reactant1-(Diphenylmethoxy)-3-bromopropaneHCID 14306367—
SolventDimethylformamideHCID 6228—
Product1-[3-(Diphenylmethoxy)propyl] 3-(3-methoxyphenyl)pyrrolidineHCID 1455630951.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 5.3 g (50 mmole) of 1-(diphenylmethoxy)-3-bromopropane in 50 cm3 of dimethylformamide was added to a mixture of 8.8 g (50 mmole) of 3-(3-methoxyphenyl)pyrrolidine, 13.8 g (100 mmole) of potassium carbonate, a few potassium iodide crystals and 250 cm3 of dimethylformamide. The reactive medium was heated to 80° C. for 12 hours and then filtered after it returned to room temperature. The filtrate was concentrated to dryness under reduced pressure. The residue was taken up with ether and extracted with 500 cm3 of N hydrochloric acid. The aqueous phase was separated, basified with 10N sodium hydroxide solution and extracted with methylene chloride. The organic solution was dried on sodium sulfate. Evaporation of the solvent yielded an oily residue, which was purified by silica gel column filtration (eluent, hexane-ethyl acetate, 1/1). There was obtained 10.3 g (yield: 51.3%) of 1-[3-(diphenylmethoxy)propyl] 3-(3-methoxyphenyl)pyrrolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04957927
Source datasetuspto-grants-1990_09
ORD IDord-ffb1ceabd32a4e57b42e4156244a95cc
Source noteuspto-grants-1990_09