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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818833Generated: November 1, 2026

1-Fluoro-2-nitrobenzene → 3,4-difluoro-N-(2-nitrophenyl)aniline

https://huagongshe.com/reaction/1818833

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant3,4-DifluoroanilineHCID 77469—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3,4-difluoro-N-(2-nitrophenyl)anilineHCID 5956076891%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 3,4-difluoroaniline (10.0 mL, 1.0 mol) in tetrahydrofuran (200 mL) was cooled to −78° C., treated with n-butyllithium solution (44 mL of a 2.5 M hexanes solution, 1.1 mol), stirred at −78° C. for 1 h and then warmed to 0° C. for 30 min. The reaction mixture was cooled to −78° C. and 1-fluoro-2-nitrobenzene (9.5 mL, 0.9 mol) in tetrahydrofuran (10 mL) was slowly added and the reaction, after which the reaction was warmed to room temperature. The reaction mixture was evaporated to provide 3,4-difluoro-N-(2-nitrophenyl)aniline (22.76 g, 91%) as a brown solid. The crude product was taken on to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601722B2
Source datasetuspto-grants-2009_10
ORD IDord-9a654d86d53e4deaab660f060a207f0a
Source noteuspto-grants-2009_10