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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188155Generated: November 2, 2026

Iodoethane → 3-(3,4-Difluorophenyl)-1-ethyl-3-methoxypyrrolidine

https://huagongshe.com/reaction/1188155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(3,4-Difluorophenyl)-3-methoxypyrrolidineHCID 46219221—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product3-(3,4-Difluorophenyl)-1-ethyl-3-methoxypyrrolidineHCID 4621922246.6%

Reaction Steps

To a solution of 3-(3,4-difluorophenyl)-3-methoxypyrrolidine (0.19 g, 0.89 mmol) in acetonitrile (5 ml), potassium carbonate (0.17 g, 1.25 mmol) and iodoethane (0.075 ml, 0.94 mmol) was added and the mixture was stirred at ambient temperature for 5 h. Aqueous sodiumcarbonate (10%, 50 ml) and ethyl acetate (50 ml) was added and the organic phase was collected. The aqueous phase was extracted with ethyl acetate (2×50 ml) and the combined organic phase was washed with Brine, dried (Na2SO4) and evaporated to give the crude product. Purification on a Biotage Isolute SCX-3 SPE column (washed with methanol and eluted with methanol/triethylamine, 4:1) followed by flash column chromatography on silica gel (EtOAc/MeOH 4:1) gave the title compound (0.10 g, 46%). The amine was converted to the oxalic acid salt and recrystallized from methanol/diethyl ether: M.p. 135-136° C. MS m/z (rel. intensity, 70 eV) 241 (4), 226 (27), 211(17), 141 (26), 71 (bp).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673962B2
Source datasetuspto-grants-2014_03
ORD IDord-5c34c117cc944187a3aab3075310f21e
Source noteuspto-grants-2014_03