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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409675Generated: October 30, 2026

2-Fluoro-4-nitrophenol → 1-[2-(2-Fluoro-4-nitrophenoxy)ethyl]pyrrolidine

https://huagongshe.com/reaction/409675

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-4-nitrophenolHCID 9825—
ReactantCesium carbonateHCID 10796—
Reactant1-(2-Chloroethyl)pyrrolidine hydrochlorideHCID 81668—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-[2-(2-Fluoro-4-nitrophenoxy)ethyl]pyrrolidineHCID 25248766—

Reaction Conditions

Temperature80 °C

Reaction Steps

1-(2-Chloro-ethyl)-pyrrolidine hydrochloride (1.2 g, 7.0 mmol, 1.1 equiv) is added to a suspension of 2-fluoro-4-nitrophenol (1 g, 6.4 mmol) and cesium carbonate (5.2 g, 15.9 mmol, 2.5 equiv) in DMF (20 mL). The resulting mixture is heated to 80° C. and stirred for 18 h. Additional 1-(2-chloro-ethyl)-pyrrolidine hydrochloride (1 g) is added and the mixture is stirred for 3 h at 80° C. The reaction mixture is cooled to RT, diluted with EtOAc and H2O. The layers are separated and the aqueous layer is extracted with EtOAc. The organic phase is washed with H2O, dried (Na2SO4), filtered and concentrated. The residue is purified by silica gel column chromatography (DCM/MeOH+1% NH3aq, 95:5) to provide the title compound as a yellow solid. ESI-MS: 255.1 [MH]+; tR=2.57 min (system 1); TLC: Rf=0.55 (DCM/MeOH+1% NH3aq, 95:5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759517B2
Source datasetuspto-grants-2014_06
ORD IDord-b49b29c0bd664e96a6649bafb1055bae
Source noteuspto-grants-2014_06