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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931810Generated: October 26, 2026

Iodoethane → 3-(3-Chloro-2-fluorophenyl)-1-ethylpyrrolidin-3-ol

https://huagongshe.com/reaction/1931810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(3-Chloro-2-fluorophenyl)pyrrolidin-3-olHCID 68515744—
SolventAcetonitrileHCID 6342—
Product3-(3-Chloro-2-fluorophenyl)-1-ethylpyrrolidin-3-olHCID 25143670—

Reaction Conditions

Temperature120 °C

Reaction Steps

In a sealed tube a mixture of 3-(3-chloro-2-fluorophenyl)pyrrolidin-3-ol (0.5 g, 2.32 mmol), acetonitrile (3 mL), potassium carbonate (0.48 g, 3.48 mmol) and iodoethane (0.36 g, 2.32 mmol) was heated under microwave irradiation at 120° C. for 20 minutes. Aqueous sodium carbonate (10%, 50 mL) was added and the aqueous phase was extracted with ethyl acetate (2×50 mL). The combined organic phase was dried (Na2SO4) and evaporated. Purification by HPLC on Waters OBD C18, 5 μm (MeOH/33 mM NH3, 20:80 to 50:50) gave the title compound. The amine was converted to the fumaric acid salt and recrystallized from methanol/diethyl ether/diisopropyl ether (0.249 g). M.p. 142-145.5° C.; MS m/z (relative intensity, 70 eV) 243 (M+, 24), 228 (19), 157 (15), 72 (27), 71 (bp).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188301B2
Source datasetuspto-grants-2012_05
ORD IDord-28bc2775f5854e0bbe554760e6ed6712
Source noteuspto-grants-2012_05