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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931814Generated: October 26, 2026

Iodoethane → 3-(3,4-Difluorophenyl)-1-ethylpyrrolidin-3-ol

https://huagongshe.com/reaction/1931814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(3,4-Difluorophenyl)pyrrolidin-3-olHCID 63586972—
SolventAcetonitrileHCID 6342—
Product3-(3,4-Difluorophenyl)-1-ethylpyrrolidin-3-olHCID 2514366239.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a sealed tube a mixture of enantiomer E1 of 3-(3,4-difluorophenyl)pyrrolidin-3-ol (0.26 g, 1.3 mmol), acetonitrile (3 mL), potassium carbonate (0.269 g, 1.95 mmol) and iodoethane (0.20 g, 1.3 mmol) was heated under microwave irradiation at 80° C. for 25 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 washed with brine, dried (Na2SO4) and evaporated. Purification by HPLC on Waters OBD C18, 5 μm (MeOH/33 mM NH3, 35:65 to 50:50) gave the title compound (0.117 g). [α]D=+19.4° (methanol). The amine was converted to the fumaric acid salt and recrystallized from methanol/diethyl ether/diisopropyl ether: M.p. 136-137° C.; MS m/z (relative intensity, 70 eV) 227 (M+, 10), 207, (19), 141 (20), 72 (42), 71 (bp).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188301B2
Source datasetuspto-grants-2012_05
ORD IDord-5ec5579c2add408180d4fd5cb0c26ce0
Source noteuspto-grants-2012_05