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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446113Generated: October 29, 2026

2-Pyrrolidone → 1-(2-Fluoro-4-nitrophenyl)-2-pyrrolidinone

https://huagongshe.com/reaction/1446113

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyrrolidoneHCID 12025—
ReactantSodium hydrideHCID 24758—
Reactant1,2-Difluoro-4-nitrobenzeneHCID 123053—
SolventDimethylformamideHCID 6228—
Product1-(2-Fluoro-4-nitrophenyl)-2-pyrrolidinoneHCID 53433965—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 468 mg (5.5 mmol) of 2-pyrrolidone (Fluka, Buchs, Switzerland) in 10 ml of DMF at 0° C. are added 240 mg (5.5 mmol) of 55% NaH in oil. The reaction mixture is stirred for 30 min at 0° C. and for 30 min at rt. After this time, 795 mg (5 mmol) of 3,4-difluoronitrobenzene (Aldrich, Buchs, Switzerland) are added and the reaction mixture is stirred for 1 h at rt. The reaction mixture is quenched with 1 M aqueous HCl and extracted with EtOAc (2×). The organic layers are washed with aqueous sat. NaHCO3 and with brine (3×), dried over MgSO4, filtered and evaporated. The residue is purified by flash chromatography on silica gel (hexane-EtOAc 5:1 to 1:3) to give the title compound as a solid. ES-MS: 225 (M+H)+; analytical HPLC: tret=2.99 minutes (Grad 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07667039B2
Source datasetuspto-grants-2010_02
ORD IDord-e4ba6d4d913147e1b50ffb53c0d9bcf3
Source noteuspto-grants-2010_02