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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595923Generated: October 31, 2026

Methyl iodide → 4-(6-Fluoropyridin-3-yl)-1-methylpyrrolidin-2-one

https://huagongshe.com/reaction/595923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-(6-Fluoropyridin-3-yl)pyrrolidin-2-oneHCID 118046426—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-(6-Fluoropyridin-3-yl)-1-methylpyrrolidin-2-oneHCID 11804583458%

Reaction Steps

To 4-(6-fluoropyridin-3-yl)pyrrolidin-2-one (200 mg, 0.888 mmol) in DMF (4 mL) in ice bath was added NaH (42.6 mg, 1.066 mmol) and iodomethane (0.067 mL, 1.066 mmol). The reaction mixture was stirred in ice bath for 30 min and room temperature for 1 hour. LC-MS shows mixture of SM and product (1:1). Added again NaH (42.6 mg, 1.066 mmol) and iodomethane (0.067 mL, 1.066 mmol), stirred for 1 h at room temperature. Complete reaction by LC-MS. Reaction mixture was diluted with EtOAc and washed with water and bine. The organic layer was dried over sodium sulfate, filtered and evaporated. The crude was purified by flash chromatography [0-50-80% EtOAc (contains 10% MeOH)/heptane]. LCMS (m/z): 195.2 (MH+), 0.492 min. Yield 58%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-3e7af4c68f7e448aacdd99f4c591b64f
Source noteuspto-grants-2016_01