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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371269Generated: October 31, 2026

4-Nitrophenethyl alcohol → 1-(2-Fluoroethyl)-4-nitrobenzene

https://huagongshe.com/reaction/1371269

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenethyl alcoholHCID 7494—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product1-(2-Fluoroethyl)-4-nitrobenzeneHCID 14809007—

Reaction Steps

A solution of 2-(4-nitrophenyl)ethanol (835 mg) in methylene chloride (30 mL) was stirred at −78° C. under a nitrogen atomosphere. To this solution, diethylaminosulfur trifluoride (1.98 mL) in methylene chloride (20 mL) was added dropwise over 10 minutes. With stirring, the temperature of the reaction mixture was allowed to rise back to room temperature. After 30 minutes, the reaction was stopped by the addition of saturated aqueous sodium hydrogen carbonate solution (50 mL) in an ice bath. The methylene chloride solution was washed with saturated aqueous sodium hydrogen carbonate solution (50 mL). After drying over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure. The residue was purified by chromatography on a silica gel (25 g) column using hexane:ethyl acetate (7:2) as the eluant to give 1-fluoro-2-(4-nitrophenyl)ethane (359 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157442B2
Source datasetuspto-grants-2007_01
ORD IDord-797e93aa1ccb49db8a3e3ff7a245dcc9
Source noteuspto-grants-2007_01